Canonical Allele Identifier: PA2829542653
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 2850528
ClinVar RCV Id: RCV003630877

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004534.3:p.Ser4246Asn
CA1908095
NM_004543.5:c.12737G>A