Canonical Allele Identifier: PA2826381274
Gene: HPGD HGNC NCBI

Linked Data

ClinVar Variation Id: 1525167
ClinVar RCV Id: RCV002032259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243235.1:p.Tyr149Cys
CA3142201
NM_001256306.2:c.446A>G