Canonical Allele Identifier: PA2828503041
Gene: SPAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410995

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361250.1:p.Lys755Asn
CA4827704
NM_001374321.1:c.2265A>T
CA371817285
NM_001374321.1:c.2265A>C