Canonical Allele Identifier: PA349386
Gene: SERPINB13 HGNC NCBI

Linked Data

ClinVar Variation Id: 219298
ClinVar RCV Id: RCV000205201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294852.1:p.Ala307Val
CA349384
NM_001307923.2:c.920C>T