Canonical Allele Identifier: PA2825403526
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 418428
ClinVar RCV Id: RCV000484673 RCV001084808 RCV001335064 RCV001272680 RCV003902722
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035931.1:p.Leu137Val
CA5547774
NM_001042466.3:c.409C>G