Canonical Allele Identifier: PA645380321
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428374
ClinVar RCV Id: RCV000491991 RCV000523733 RCV000792665
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile502Thr
CA067775
NM_000179.3:c.1505T>C