Canonical Allele Identifier: PA2825403440
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 300534
ClinVar RCV Id: RCV000279820 RCV000333853 RCV000334914 RCV000388278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035931.1:p.Thr38Ser
CA5547902
NM_001042466.3:c.112A>T