Canonical Allele Identifier: PA2829413945
Gene: SPAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003105.2:p.Ala238Val
CA4827344
NM_003114.5:c.713C>T