Canonical Allele Identifier: PA645511154
Gene: CORIN HGNC NCBI

Linked Data

ClinVar Variation Id: 439552
ClinVar RCV Id: RCV000506762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006578.2:p.Ser542Thr
CA2909614
NM_006587.4:c.1624T>A