Canonical Allele Identifier: PA2825454078
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 355299
ClinVar RCV Id: RCV000315035 RCV002520405 RCV003133245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Thr2566Ala
CA3994640
NM_001079823.2:c.7696A>G