Canonical Allele Identifier: PA272269
Gene: NIPBL HGNC NCBI

Linked Data

ClinVar Variation Id: 159212
ClinVar RCV Id: RCV000146706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056199.2:p.Gly2312Val
CA272268
NM_015384.5:c.6935G>T