Canonical Allele Identifier: PA915970532
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 13365
ClinVar RCV Id: RCV000014294 RCV000014293 RCV001857349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002769.1:p.Met1Leu