Canonical Allele Identifier: PA915984899
Gene: HPD HGNC NCBI

Linked Data

ClinVar Variation Id: 1576
ClinVar RCV Id: RCV000001642 RCV000386406 RCV000953322 RCV001091863 RCV003964786 RCV003488319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002141.2:p.Ile335Met
CA115065
NM_002150.3:c.1005C>G