Canonical Allele Identifier: PA2825403421
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1442678
ClinVar RCV Id: RCV001960333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035931.1:p.Pro18Ala
CA209472135
NM_001042466.3:c.52C>G