Canonical Allele Identifier: PA2826606947
Gene: CORIN HGNC NCBI

Linked Data

ClinVar Variation Id: 439552
ClinVar RCV Id: RCV000506762
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265514.1:p.Ser438Thr
CA2909614
NM_001278585.2:c.1312T>A