Canonical Allele Identifier: PA2829382354
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 300514
ClinVar RCV Id: RCV000349589 RCV000350842 RCV000389048 RCV001044241 RCV001833438 RCV002262951 RCV002520627
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002769.1:p.Thr391Met
CA5547470
NM_002778.4:c.1172C>T