Canonical Allele Identifier: PA2580276385
Gene: LAMB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2067243
ClinVar RCV Id: RCV002966351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002282.2:p.Ser521Thr
CA368874745
NM_002291.3:c.1562G>C