Canonical Allele Identifier: PA2826381268
Gene: HPGD HGNC NCBI

Linked Data

ClinVar Variation Id: 1502096
ClinVar RCV Id: RCV002010896 RCV002642151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243235.1:p.Glu127Ala
CA3142216
NM_001256306.2:c.380A>C