Canonical Allele Identifier: PA658659892
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 445595
ClinVar RCV Id: RCV000514444 RCV001081218 RCV001272678 RCV003962415
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002769.1:p.Ile208Ser
CA5547714
NM_002778.4:c.623T>G