Canonical Allele Identifier: PA2825454059
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1401419
ClinVar RCV Id: RCV001911800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Leu2561Ser
CA365628251
NM_001079823.2:c.7682T>C