Canonical Allele Identifier: PA2825166488
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 557960
ClinVar RCV Id: RCV000674166 RCV001063982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Gln28dup
CA658823178
NM_000426.4:c.83_85dup