Canonical Allele Identifier: PA915984889
Gene: HPD HGNC NCBI

Linked Data

ClinVar Variation Id: 307484
ClinVar RCV Id: RCV000270114 RCV000362382 RCV000967705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002141.2:p.Met166Ile
CA6839638
NM_002150.3:c.498G>A
CA387017316
NM_002150.3:c.498G>T
CA387017323
NM_002150.3:c.498G>C