Canonical Allele Identifier: PA272055
Gene: NIPBL HGNC NCBI

Linked Data

ClinVar Variation Id: 159079
ClinVar RCV Id: RCV000146572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597677.2:p.Ser111Asn
CA272053
NM_133433.4:c.332G>A