ClinGen Allele Registry
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Canonical Allele Identifier:
PA115066
Gene: HPD
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
16615
ClinVar RCV:
RCV000001642
RCV000386406
RCV000953322
RCV001091863
RCV003488319
RCV003964786
ClinVar Variation:
1576
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001165464.1:p.Ile296Met
CA115065
NM_001171993.2:c.888C>G