Canonical Allele Identifier: PA2825363284
Gene: SPATA7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1058010
ClinVar RCV Id: RCV001367097
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Amino-acid Alleles

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