Canonical Allele Identifier: PA2741960540
Gene: NME8 HGNC NCBI
ClinVar RCV:
RCV003501922
ClinVar Variation:
2745433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057700.3:p.Pro84Ala
CA367220192
NM_016616.5:c.250C>G