Canonical Allele Identifier: PA2499229286
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala322Thr
CA073662
NM_000179.3:c.964G>A