Canonical Allele Identifier: PA116529
Gene: SERPING1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3954
ClinVar RCV Id: RCV000004160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000053.2:p.Gly453delinsValTrp
CA116527
NM_000062.3:c.1357_1358insTGT