Canonical Allele Identifier: PA2826381111
Gene: HPGD HGNC NCBI

Linked Data

ClinVar Variation Id: 7917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243230.1:p.Ala19Pro
CA119153
NM_001256301.1:c.55G>C