Canonical Allele Identifier: PA2826606942
Gene: CORIN HGNC NCBI

Linked Data

ClinVar Variation Id: 161648
ClinVar RCV Id: RCV000149184
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265514.1:p.Pro363Arg
CA174525
NM_001278585.2:c.1088C>G