Canonical Allele Identifier: PA915967650
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 435714
ClinVar RCV Id: RCV000500474 RCV000557131 RCV000764632 RCV001509285 RCV004541559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Thr2363Ile
CA3994438
NM_001079823.2:c.7088C>T