Canonical Allele Identifier: PA658663058
Gene: SPATA7 HGNC NCBI

Linked Data

ClinVar Variation Id: 427862
ClinVar RCV Id: RCV000515659
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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