Canonical Allele Identifier: PA915965253
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 648235

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gln1314Glu
CA346761500
NM_000179.3:c.3940C>G