Canonical Allele Identifier: PA2741830156
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2689356
ClinVar RCV Id: RCV003487996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Gly1243Arg
CA365613130
NM_001079823.2:c.3727G>A
CA365613132
NM_001079823.2:c.3727G>C