Canonical Allele Identifier: PA107222
Gene: PSAP HGNC NCBI

Linked Data

ClinVar Variation Id: 13363
ClinVar RCV Id: RCV000588928 RCV004527289 RCV000014291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002769.1:p.Cys241Ser
CA123057
NM_002778.4:c.722G>C
CA377149657
NM_002778.4:c.721T>A