Canonical Allele Identifier: PA2825167618
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1501770
ClinVar RCV Id: RCV002010810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Gly1209Asp
CA365612806
NM_000426.4:c.3626G>A