Canonical Allele Identifier: PA2826628908
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89457
ClinVar RCV Id: RCV000160699 RCV000212689 RCV000408995 RCV000524187 RCV000587284 RCV004537280 RCV003997096
ClinVar Variation Id: 1734684
ClinVar RCV Id: RCV002349379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu1124Asp
CA014214
NM_001281492.2:c.3372A>T
CA346761105
NM_001281492.2:c.3372A>C