Canonical Allele Identifier: PA2828435568
Gene: PSPH HGNC NCBI

Linked Data

ClinVar Variation Id: 13624
ClinVar RCV Id: RCV000014594

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357442.1:p.Met52Thr
CA123296
NM_001370513.1:c.155T>C