Canonical Allele Identifier: PA915972979
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 533993
ClinVar RCV Id: RCV000641337 RCV001662690 RCV002507092
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004534.3:p.Arg2437Trp
CA1909881
NM_004543.5:c.7309C>T