Canonical Allele Identifier: PA2741891820
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2504904
ClinVar RCV Id: RCV003234495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002281.3:p.Ala19Val
CA3966350
NM_002290.4:c.56C>T