Canonical Allele Identifier: PA2825403564
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 300525
ClinVar RCV Id: RCV000291043 RCV000345936 RCV000391944 RCV000401145
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035931.1:p.Arg186His
CA5547747
NM_001042466.3:c.557G>A