Canonical Allele Identifier: PA2826624666
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1769374
ClinVar RCV Id: RCV002380812 RCV003465713 RCV003594253 RCV004007300
ClinVar Variation Id: 1769379
ClinVar RCV Id: RCV002380817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gln4His
CA346734479
NM_001281492.2:c.12G>C
CA346734480
NM_001281492.2:c.12G>T