Canonical Allele Identifier: PA1139673115
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 935393
ClinVar RCV Id: RCV001203974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Glu614Lys
CA365609584
NM_001079823.2:c.1840G>A