Canonical Allele Identifier: PA2826104546
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_001165464.1:p.Val301Leu
CA6839439
NM_001171993.2:c.901G>T
CA387008902
NM_001171993.2:c.901G>C