Canonical Allele Identifier: PA915972076
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 533979
ClinVar RCV Id: RCV000641321 RCV003148813 RCV003488752 RCV003472031
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004534.3:p.Asp498Gly
CA348825220
NM_004543.5:c.1493A>G