Canonical Allele Identifier: PA658663058
Gene: SPATA7 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060888.2:p.Glu405Asp
CA7298763
NM_018418.5:c.1215G>T
CA390570754
NM_018418.5:c.1215G>C