Canonical Allele Identifier: PA2825168426
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 376977
ClinVar RCV Id: RCV000422473 RCV000672201 RCV002524713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Lys2067del
CA3994132
NM_000426.4:c.6201_6203del