Canonical Allele Identifier: PA2825551658
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2504904
ClinVar RCV Id: RCV003234495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098677.2:p.Ala19Val
CA3966350
NM_001105207.3:c.56C>T