Canonical Allele Identifier: PA2825403129
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 521912
ClinVar RCV Id: RCV000624741 RCV001731817
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035930.1:p.Ile86Asn
CA377154031
NM_001042465.3:c.257T>A