Canonical Allele Identifier: PA2828502927
Gene: SPAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410994
ClinVar RCV Id: RCV000463219 RCV002365656 RCV003932713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361250.1:p.Thr409Ser
CA4827471
NM_001374321.1:c.1226C>G
CA371808984
NM_001374321.1:c.1225A>T