Canonical Allele Identifier: PA2829543324
Gene: NEB HGNC NCBI
ClinVar RCV:
RCV002750571
ClinVar Variation:
1973518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004534.3:p.Arg4776Ser
CA348791913
NM_004543.5:c.14326C>A