Canonical Allele Identifier: PA1139678871
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 877049
ClinVar RCV Id: RCV001102474 RCV004032088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121113.1:p.Phe506Ile
CA1375557
NM_001127641.1:c.1516T>A