Canonical Allele Identifier: PA2825089387
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2453191
ClinVar RCV Id: RCV003182646 RCV004009649
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr750Pro
CA346752643
NM_000179.3:c.2248A>C