Canonical Allele Identifier: PA115057
Gene: HPD HGNC NCBI

Linked Data

ClinVar Variation Id: 1573
ClinVar RCV Id: RCV000001639 RCV001297386 RCV001731268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165464.1:p.Tyr121Cys
CA115056
NM_001171993.2:c.362A>G