Canonical Allele Identifier: PA2580264770
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1984846
ClinVar RCV Id: RCV002775702
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002769.1:p.Gly17Ser
CA5547921
NM_002778.4:c.49G>A