Canonical Allele Identifier: PA915967546
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 295151
ClinVar RCV Id: RCV000294349 RCV000892333 RCV001526759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121113.1:p.Arg23Cys
CA1376110
NM_001127641.1:c.67C>T
CA645516431
NM_001127641.1:c.66_67delinsTT