Canonical Allele Identifier: PA2828502895
Gene: SPAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1438839
ClinVar RCV Id: RCV001949084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361250.1:p.Asp304Gly
CA4827399
NM_001374321.1:c.911A>G