Canonical Allele Identifier: PA2741960551
Gene: NME8 HGNC NCBI
ClinVar RCV:
RCV003608538
ClinVar Variation:
2884808
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057700.3:p.Asp137Val
CA4222181
NM_016616.5:c.410A>T