Canonical Allele Identifier: PA2826627110
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_001268421.1:p.Asp633Asn
CA346752932
NM_001281492.2:c.1897G>A