Canonical Allele Identifier: PA645463836
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 295078
ClinVar RCV Id: RCV000318642 RCV002519479 RCV003391057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000219.2:p.Asn944Ser
CA1375086
NM_000228.3:c.2831A>G