Canonical Allele Identifier: PA658654056
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 444224
ClinVar RCV Id: RCV000512836 RCV001087790 RCV001834647 RCV003960205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035930.1:p.Leu4Val
CA5547944
NM_001042465.3:c.10C>G