Canonical Allele Identifier: PA2580148427
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1945110
ClinVar RCV Id: RCV002640086 RCV002640085 RCV003130741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Leu595Phe
CA3992748
NM_001079823.2:c.1783C>T