Canonical Allele Identifier: PA915967527
Gene: LAMA2 HGNC NCBI
ClinVar Allele:
521393
ClinVar RCV:
RCV000654759
ClinVar Variation:
543876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Lys2117Arg
CA3994248
NM_001079823.2:c.6350A>G