Canonical Allele Identifier: PA2828502819
Gene: SPAG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 88680
ClinVar RCV Id: RCV000074363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361250.1:p.Met1Arg