Canonical Allele Identifier: PA645436973
Gene: SPAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_757367.1:p.Thr409Ser
CA4827471
NM_172218.3:c.1226C>G
CA371808984
NM_172218.3:c.1225A>T