Canonical Allele Identifier: PA2826104559
Gene: HPD HGNC NCBI

Linked Data

ClinVar Variation Id: 812775
ClinVar RCV Id: RCV001003605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165464.1:p.Val311Ala
CA387008762
NM_001171993.2:c.932T>C