Canonical Allele Identifier: PA2826470244
Gene: SPATA20 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245302.1:p.Glu545Asp
CA8651656
NM_001258373.2:c.1635G>C
CA400249420
NM_001258373.2:c.1635G>T