Canonical Allele Identifier: PA232162
Gene: LIN28B HGNC NCBI

Linked Data

ClinVar Variation Id: 91920
ClinVar RCV Id: RCV000122477
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001004317.1:p.Ala2Asp
CA232161
NM_001004317.4:c.5C>A