Canonical Allele Identifier: PA915970559
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 444223
ClinVar RCV Id: RCV000513446 RCV001088093 RCV001829458 RCV004023457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002769.1:p.Gly43Glu
CA5547892
NM_002778.4:c.128G>A