Canonical Allele Identifier: PA2829414219
Gene: SPAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410995

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003105.2:p.Lys755Asn
CA4827704
NM_003114.5:c.2265A>T
CA371817285
NM_003114.5:c.2265A>C