Canonical Allele Identifier: PA2825986295
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_001157979.2:p.Met7483Leu
CA348764677
NM_001164507.2:c.22447A>T
CA348764682
NM_001164507.2:c.22447A>C