Canonical Allele Identifier: PA2829382280
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 300515
ClinVar RCV Id: RCV000301263 RCV000335258 RCV000390963 RCV000390949 RCV001356155 RCV001828310
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002769.1:p.Thr363Met
CA5547484
NM_002778.4:c.1088C>T