Canonical Allele Identifier: PA915967857
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 295070
ClinVar RCV Id: RCV000306429 RCV000903505 RCV003940103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121113.1:p.Arg1042Trp
CA1374973
NM_001127641.1:c.3124C>T