Canonical Allele Identifier: PA2825403169
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 418428
ClinVar RCV Id: RCV000484673 RCV001084808 RCV001335064 RCV001272680 RCV003902722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035930.1:p.Leu137Val
CA5547774
NM_001042465.3:c.409C>G