Canonical Allele Identifier: PA2573177230
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1348842
ClinVar RCV Id: RCV002046633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Ala1201Val
CA365612729
NM_001079823.2:c.3602C>T