Canonical Allele Identifier: PA2825552970
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2062170
ClinVar RCV Id: RCV002953231

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098679.1:p.Ala2Val
CA365519039
NM_001105209.3:c.5C>T