Canonical Allele Identifier: PA2499229394
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1025897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met662Lys
CA346750633
NM_000179.3:c.1985T>A