Canonical Allele Identifier: PA2826381266
Gene: HPGD HGNC NCBI

Linked Data

ClinVar Variation Id: 2689223
ClinVar RCV Id: RCV003487909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243235.1:p.Val108Met
CA3142222
NM_001256306.2:c.322G>A