Canonical Allele Identifier: PA915988589
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 644453
ClinVar RCV Id: RCV000798371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Ser1472Thr
CA352693150
NM_002292.4:c.4415G>C