Canonical Allele Identifier: PA174526
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_006578.2:p.Pro467Arg
CA174525
NM_006587.4:c.1400C>G