Canonical Allele Identifier: PA915963625
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 822941
ClinVar RCV Id: RCV001018720
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg302Gly
CA346740708
NM_000179.3:c.904A>G