Canonical Allele Identifier: PA2826635842
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233402
ClinVar RCV Id: RCV000219205 RCV001327131
ClinVar Variation Id: 1047397
ClinVar RCV Id: RCV001352101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Phe424Leu
CA10578096
NM_001281494.2:c.1270T>C
CA346751201
NM_001281494.2:c.1272C>A
CA346751203
NM_001281494.2:c.1272C>G