Canonical Allele Identifier: PA2826470261
Gene: SPATA20 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245302.1:p.Arg737Gln
CA400251761
NM_001258373.2:c.2210G>A