Canonical Allele Identifier: PA645413980
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 300515
ClinVar RCV Id: RCV000301263 RCV000335258 RCV000390963 RCV000390949 RCV001356155 RCV001828310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035930.1:p.Thr366Met
CA5547484
NM_001042465.3:c.1097C>T