Canonical Allele Identifier: PA2826626628
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1195062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly520Asp
CA346750527
NM_001281492.2:c.1559G>A