Canonical Allele Identifier: PA913192049
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 628779
ClinVar RCV Id: RCV000773442
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly45Val
CA346734899
NM_000179.3:c.134G>T