Allele Registry

Canonical Allele Identifier: PA2825363284

Gene: SPATA7 HGNC NCBI

ClinVar RCV:

RCV001367097

ClinVar Variation:

1058010

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035518.1:p.Ser4Arg	CA390543409 NM_001040428.4:c.10A>C CA390543436 NM_001040428.4:c.12C>G CA390543437 NM_001040428.4:c.12C>A