Canonical Allele Identifier: PA913192127
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 619576
ClinVar RCV Id: RCV000758667
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp763Asn
CA346752932
NM_000179.3:c.2287G>A