Canonical Allele Identifier: PA645384157
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410425

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu1177Val
CA071122
NM_000179.3:c.3529C>G