Canonical Allele Identifier: PA2825981539
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 2202344
ClinVar RCV Id: RCV002629954 RCV003130864
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157979.2:p.Met1395Ile
CA57651061
NM_001164507.2:c.4185G>A
CA348816612
NM_001164507.2:c.4185G>T
CA348816613
NM_001164507.2:c.4185G>C