Canonical Allele Identifier: PA658815520
Gene: NME8 HGNC NCBI
ClinVar RCV:
RCV000645500
ClinVar Variation:
536824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057700.3:p.Thr30Ala
CA4222040
NM_016616.5:c.88A>G