Canonical Allele Identifier: PA915967639
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 384649
ClinVar RCV Id: RCV000551529 RCV001698140 RCV003372705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Arg2353His
CA3994428
NM_001079823.2:c.7058G>A