Canonical Allele Identifier: PA2825551122
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2978442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098676.2:p.Trp7Leu
CA365519008
NM_001105206.3:c.20G>T