Canonical Allele Identifier: PA2826607039
Gene: CORIN HGNC NCBI

Linked Data

ClinVar Variation Id: 161648
ClinVar RCV Id: RCV000149184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265515.1:p.Pro430Arg
CA174525
NM_001278586.2:c.1289C>G