Canonical Allele Identifier: PA2826626371
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 568393
ClinVar RCV Id: RCV000688742 RCV002397381
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro461Gln
CA346749161
NM_001281492.2:c.1382C>A