Canonical Allele Identifier: PA916011280
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141346
ClinVar RCV Id: RCV000129832 RCV000221076 RCV000410297 RCV001298939 RCV003997528
ClinVar Variation Id: 182642
ClinVar RCV Id: RCV000160689 RCV000564450 RCV000691133
ClinVar Variation Id: 1020779
ClinVar RCV Id: RCV001320413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe907Leu
CA011575
NM_001281492.2:c.2721C>A
CA011584
NM_001281492.2:c.2721C>G
CA346756610
NM_001281492.2:c.2719T>C