Canonical Allele Identifier: PA1139672626
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_001073291.2:p.Gln28dup
CA658823178
NM_001079823.2:c.83_85dup