Canonical Allele Identifier: PA2825086776
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1759382
ClinVar RCV Id: RCV002393882
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile251Thr
CA346740130
NM_000179.3:c.752T>C