Canonical Allele Identifier: PA2741830341
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2527641
ClinVar RCV Id: RCV003242004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.His2397Pro
CA146892057
NM_001079823.2:c.7190A>C