Canonical Allele Identifier: PA915967685
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 594686
ClinVar RCV Id: RCV000730036

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Ile2430Leu
CA365622200
NM_001079823.2:c.7288A>C