Canonical Allele Identifier: PA2826634308
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1045496
ClinVar RCV Id: RCV001349917
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr25Asn
CA346741019
NM_001281494.2:c.74C>A