Canonical Allele Identifier: PA2825551157
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 492988

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098676.2:p.Asp35Glu
CA3966336
NM_001105206.3:c.105C>G
CA365518833
NM_001105206.3:c.105C>A