Canonical Allele Identifier: PA092990
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 18032
ClinVar RCV Id: RCV000019648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000479.1:p.Ser381Pro
CA210783
NM_000488.4:c.1141T>C