Canonical Allele Identifier: PA645437009
Gene: SPAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410995

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_757367.1:p.Lys755Asn
CA4827704
NM_172218.3:c.2265A>T
CA371817285
NM_172218.3:c.2265A>C