Canonical Allele Identifier: PA915988417
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 659645
ClinVar RCV Id: RCV000816675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Cys954Trp
CA352715826
NM_002292.4:c.2862C>G