Canonical Allele Identifier: PA2826470252
Gene: SPATA20 HGNC NCBI
ClinVar RCV:
RCV004194602
ClinVar Variation:
2352354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245302.1:p.Pro640Leu
CA8651745
NM_001258373.2:c.1919C>T