Canonical Allele Identifier: PA1139674621
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 936443
ClinVar RCV Id: RCV001205241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Lys2421Arg
CA365622074
NM_001079823.2:c.7262A>G