Canonical Allele Identifier: PA2829992734
Gene: SPATA20 HGNC NCBI
ClinVar RCV:
RCV004460160
ClinVar Variation:
3168246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073738.2:p.Ala398Thr
CA8651433
NM_022827.3:c.1192G>A