Canonical Allele Identifier: PA2741891960
Gene: LAMB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2986700
ClinVar RCV Id: RCV003846355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002282.2:p.Ser1478Thr
CA368864180
NM_002291.3:c.4433G>C