Canonical Allele Identifier: PA123070
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 13372
ClinVar RCV Id: RCV000014301 RCV003317034
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035930.1:p.Leu352Pro
CA123069
NM_001042465.3:c.1055T>C