Canonical Allele Identifier: PA115066
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_001165464.1:p.Ile296Met
CA115065
NM_001171993.2:c.888C>G