Canonical Allele Identifier: PA2829544541
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 1929162
ClinVar RCV Id: RCV002618593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004534.3:p.Met5782Leu
CA348764677
NM_004543.5:c.17344A>T
CA348764682
NM_004543.5:c.17344A>C