Canonical Allele Identifier: PA1139701492
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 989891
ClinVar RCV Id: RCV001277794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002769.1:p.Ala14Val
CA377156411
NM_002778.4:c.41C>T