Canonical Allele Identifier: PA2580413337
Gene: NME8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1980757
ClinVar RCV Id: RCV002761578
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057700.3:p.Gln430Arg
CA4222490
NM_016616.5:c.1289A>G