Canonical Allele Identifier: PA915966988
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 194173
ClinVar RCV Id: RCV000174479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Glu628Lys
CA240014
NM_001079823.2:c.1882G>A