Canonical Allele Identifier: PA645436965
Gene: SPAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_757367.1:p.Ala238Val
CA4827344
NM_172218.3:c.713C>T