Canonical Allele Identifier: PA1139708427
Gene: HPD HGNC NCBI

Linked Data

ClinVar Variation Id: 936109
ClinVar RCV Id: RCV001204845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002141.2:p.Gly260Arg
CA6839534
NM_002150.3:c.778G>A
CA387012806
NM_002150.3:c.778G>C