Canonical Allele Identifier: PA2825087320
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 918559
ClinVar RCV Id: RCV001176217
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr305Pro
CA346740723
NM_000179.3:c.913A>C