Canonical Allele Identifier: PA2826470169
Gene: SPATA20 HGNC NCBI
ClinVar RCV:
RCV004460160
ClinVar Variation:
3168246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245301.1:p.Ala382Thr
CA8651433
NM_001258372.2:c.1144G>A