Canonical Allele Identifier: PA2826635235
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1722242
ClinVar RCV Id: RCV002302386
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Tyr287Asn
CA346749090
NM_001281494.2:c.859T>A