Canonical Allele Identifier: PA916011001
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_001268421.1:p.Gly45Val
CA346734899
NM_001281492.2:c.134G>T