Canonical Allele Identifier: PA2829992753
Gene: SPATA20 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073738.2:p.Arg797Gln
CA400251761
NM_022827.3:c.2390G>A