Canonical Allele Identifier: PA2825802411
Gene: SPATA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2246777
ClinVar RCV Id: RCV004106448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129245.1:p.Asp333His
CA408948918
NM_001135773.2:c.997G>C