Canonical Allele Identifier: PA891846029
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 573535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg33Leu
CA346734830
NM_000179.3:c.98G>T