Canonical Allele Identifier: PA2826104519
Gene: HPD HGNC NCBI

Linked Data

ClinVar Variation Id: 307480
ClinVar RCV Id: RCV000297722 RCV000400625 RCV001859837 RCV001764274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165464.1:p.Thr266Met
CA6839486
NM_001171993.2:c.797C>T