Canonical Allele Identifier: PA1139674605
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 906087
ClinVar RCV Id: RCV001155017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Gly2396Arg
CA365621477
NM_001079823.2:c.7186G>A
CA365621487
NM_001079823.2:c.7186G>C