Canonical Allele Identifier: PA2825802432
Gene: SPATA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2204869
ClinVar RCV Id: RCV004072311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129245.1:p.Gly426Arg
CA9904863
NM_001135773.2:c.1276G>A
CA408946600
NM_001135773.2:c.1276G>C