Canonical Allele Identifier: PA915984901
Gene: HPD HGNC NCBI

Linked Data

ClinVar Variation Id: 307478
ClinVar RCV Id: RCV000290396 RCV000530874 RCV001642958 RCV000382932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002141.2:p.Val340Leu
CA6839439
NM_002150.3:c.1018G>T
CA387008902
NM_002150.3:c.1018G>C