Canonical Allele Identifier: PA174827
Gene: SPATA18 HGNC NCBI

Linked Data

ClinVar Variation Id: 161809
ClinVar RCV Id: RCV000149345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660306.1:p.Val331Ile
CA174826
NM_145263.4:c.991G>A