Canonical Allele Identifier: PA916009393
Gene: HPGD HGNC NCBI

Linked Data

ClinVar Variation Id: 7917
ClinVar RCV Id: RCV000008379 RCV000144084 RCV001781205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243236.1:p.Ala19Pro
CA119153
NM_001256307.2:c.55G>C