Canonical Allele Identifier: PA2580112964
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2191188
ClinVar RCV Id: RCV002616783 RCV002616782 RCV003130852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Asp2880Asn
CA3994882
NM_000426.4:c.8638G>A