Canonical Allele Identifier: PA2580264771
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2155289
ClinVar RCV Id: RCV003072262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002769.1:p.Pro18Leu
CA5547920
NM_002778.4:c.53C>T