Canonical Allele Identifier: PA2741890068
Gene: HPD HGNC NCBI

Linked Data

ClinVar Variation Id: 2523947
ClinVar RCV Id: RCV003289891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002141.2:p.Arg55Gln
CA6839799
NM_002150.3:c.164G>A