Canonical Allele Identifier: PA1139672987
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 907819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Asp539His
CA3992678
NM_001079823.2:c.1615G>C