Canonical Allele Identifier: PA2826470195
Gene: SPATA20 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245301.1:p.Pro684Leu
CA8651745
NM_001258372.2:c.2051C>T