Canonical Allele Identifier: PA2828502873
Gene: SPAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410996
ClinVar RCV Id: RCV000476762 RCV004022859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361250.1:p.Ala238Val
CA4827344
NM_001374321.1:c.713C>T