Canonical Allele Identifier: PA2829382338
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 13364
ClinVar RCV Id: RCV000014292
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002769.1:p.Cys382Phe
CA123059
NM_002778.4:c.1145G>T