Canonical Allele Identifier: PA916011447
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 823479
ClinVar RCV Id: RCV001019750
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile969Leu
CA346758468
NM_001281492.2:c.2905A>C