Canonical Allele Identifier: PA2825166478
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1018268
ClinVar RCV Id: RCV001317544 RCV003132406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Val20Ala
CA3992200
NM_000426.4:c.59T>C