Canonical Allele Identifier: PA2826626873
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1525371
ClinVar RCV Id: RCV002036634
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe576Ile
CA346750964
NM_001281492.2:c.1726T>A