Canonical Allele Identifier: PA915967711
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 295101
ClinVar RCV Id: RCV000287198 RCV000948239 RCV003165799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121113.1:p.Arg556His
CA1375498
NM_001127641.1:c.1667G>A