Canonical Allele Identifier: PA2825403487
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 521912
ClinVar RCV Id: RCV000624741 RCV001731817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035931.1:p.Ile86Asn
CA377154031
NM_001042466.3:c.257T>A