Canonical Allele Identifier: PA349385
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_036529.1:p.Ala298Val
CA349384
NM_012397.4:c.893C>T