Canonical Allele Identifier: PA2580148470
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2273095
ClinVar RCV Id: RCV002821957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Gly990Arg
CA365611147
NM_001079823.2:c.2968G>A
CA365611148
NM_001079823.2:c.2968G>C