Canonical Allele Identifier: PA2829544642
Gene: NEB HGNC NCBI
ClinVar RCV:
RCV001239197
ClinVar Variation:
964881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004534.3:p.Asp5883Asn
CA1906546
NM_004543.5:c.17647G>A