Canonical Allele Identifier: PA915972529
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 331509
ClinVar RCV Id: RCV000688136 RCV003133235 RCV002487463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004534.3:p.Pro1556Ser
CA1910565
NM_004543.5:c.4666C>T