Allele Registry

Canonical Allele Identifier: PA112490

Gene: LAMB3 HGNC NCBI

ClinVar RCV:

RCV000015653

ClinVar Variation:

14552

HGVS (amino-acid)	Matching Registered Transcripts
NP_000219.2:p.Lys207Gln	CA257287 NM_000228.3:c.619A>C