Canonical Allele Identifier: PA2826104308
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_001165464.1:p.Arg16Gln
CA6839799
NM_001171993.2:c.47G>A