Canonical Allele Identifier: PA645389381
Gene: SPATA7 HGNC NCBI

Linked Data

ClinVar Variation Id: 421702
ClinVar RCV Id: RCV000486342 RCV001085445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060888.2:p.His413Arg
CA7298781
NM_018418.5:c.1238A>G