Canonical Allele Identifier: PA2825089154
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1785111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly685Asp
CA346750765
NM_000179.3:c.2054G>A