Canonical Allele Identifier: PA2827436910
Gene: SERPINB13 HGNC NCBI

Linked Data

ClinVar Variation Id: 219298
ClinVar RCV Id: RCV000205201
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335199.1:p.Ala119Val
CA349384
NM_001348270.2:c.356C>T