Canonical Allele Identifier: PA096006
Gene: PSPH HGNC NCBI

Linked Data

ClinVar Variation Id: 13624
ClinVar RCV Id: RCV000014594
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004568.2:p.Met52Thr
CA123296
NM_004577.4:c.155T>C