Canonical Allele Identifier: PA136452
Gene: NEBL HGNC NCBI

Linked Data

ClinVar Variation Id: 45499
ClinVar RCV Id: RCV000038704 RCV000723614 RCV001085554 RCV003934929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006384.1:p.Gly202Arg
CA136450
NM_006393.3:c.604G>A
CA376103281
NM_006393.3:c.604G>C