Canonical Allele Identifier: PA915966974
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 380542
ClinVar RCV Id: RCV000426949 RCV000874720 RCV001288666 RCV004532988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Thr605Ile
CA3992752
NM_001079823.2:c.1814C>T