Canonical Allele Identifier: PA2580403082
Gene: SPATA7 HGNC NCBI
ClinVar RCV:
RCV002579064
ClinVar Variation:
2175227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060888.2:p.Asn31Asp
CA390545441
NM_018418.5:c.91A>G