Canonical Allele Identifier: PA2825403059
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 989891
ClinVar RCV Id: RCV001277794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035930.1:p.Ala14Val
CA377156411
NM_001042465.3:c.41C>T