Canonical Allele Identifier: PA2826631553
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3076143
ClinVar RCV Id: RCV004018460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Cys481Tyr
CA346753492
NM_001281493.2:c.1442G>A