Canonical Allele Identifier: PA915966970
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 430300
ClinVar RCV Id: RCV000493458 RCV000806947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Val598Ile
CA3992750
NM_001079823.2:c.1792G>A