Canonical Allele Identifier: PA2825166771
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 450302
ClinVar RCV Id: RCV000520035 RCV000764621 RCV001086334 RCV001153657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Asp316Asn
CA3992484
NM_000426.4:c.946G>A