Canonical Allele Identifier: PA2828502943
Gene: SPAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 474651

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361250.1:p.Pro436Leu
CA4827474
NM_001374321.1:c.1307C>T