Canonical Allele Identifier: PA2825209021
Gene: HPGD HGNC NCBI

Linked Data

ClinVar Variation Id: 1372083
ClinVar RCV Id: RCV001907920 RCV003164215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000851.2:p.Met213Val
CA3142202
NM_000860.6:c.637A>G