Canonical Allele Identifier: PA2828502845
Gene: SPAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 541535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361250.1:p.Leu138Pro
CA4827241
NM_001374321.1:c.413T>C