Canonical Allele Identifier: PA2825403404
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 444224
ClinVar RCV Id: RCV000512836 RCV001087790 RCV001834647 RCV003960205
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035931.1:p.Leu4Val
CA5547944
NM_001042466.3:c.10C>G