Canonical Allele Identifier: PA2825454480
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1509454
ClinVar RCV Id: RCV002017915
ClinVar Variation Id: 2895148
ClinVar RCV Id: RCV003739552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Lys2847Asn
CA3994863
NM_001079823.2:c.8541G>T
CA365634719
NM_001079823.2:c.8541G>C