Canonical Allele Identifier: PA658801993
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly308Asp
CA346740744
NM_000179.3:c.923G>A