Canonical Allele Identifier: PA195116
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg901Cys
CA010754
NM_000179.3:c.2701C>T