Canonical Allele Identifier: PA2825166943
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 14298
ClinVar RCV Id: RCV000015368 RCV000078747 RCV000822637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Cys527Tyr
CA123845
NM_000426.4:c.1580G>A