Canonical Allele Identifier: PA645511173
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 439202

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu758Val
CA346752834
NM_000179.3:c.2272C>G