Canonical Allele Identifier: PA2826381223
Gene: HPGD HGNC NCBI

Linked Data

ClinVar Variation Id: 156026
ClinVar RCV Id: RCV000144085 RCV003727619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243234.1:p.Met1Leu