Canonical Allele Identifier: PA2573268242
Gene: NME8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1403932
ClinVar RCV Id: RCV001925492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057700.3:p.Glu55Asp
CA367219585
NM_016616.5:c.165A>C
CA367219587
NM_016616.5:c.165A>T