Canonical Allele Identifier: PA2826470187
Gene: SPATA20 HGNC NCBI
ClinVar RCV:
RCV004233272
ClinVar Variation:
2396652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245301.1:p.Glu589Asp
CA8651656
NM_001258372.2:c.1767G>C
CA400249420
NM_001258372.2:c.1767G>T