Canonical Allele Identifier: PA2825552871
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 178049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098677.2:p.Arg1775Cys
CA295682
NM_001105207.3:c.5323C>T