Canonical Allele Identifier: PA2825802414
Gene: SPATA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2343906
ClinVar RCV Id: RCV004186094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129245.1:p.His365Arg
CA9904902
NM_001135773.2:c.1094A>G