Canonical Allele Identifier: PA2829544543
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 2164372
ClinVar RCV Id: RCV003088001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004534.3:p.Lys5785Ala
CA2580063941
NM_004543.5:c.17353_17354delinsGC