Canonical Allele Identifier: PA2580135077
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2141972
ClinVar RCV Id: RCV003058820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121113.1:p.Gly130Ser
CA1375982
NM_001127641.1:c.388G>A