Canonical Allele Identifier: PA2580276302
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2062170
ClinVar RCV Id: RCV002953231

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002281.3:p.Ala2Val
CA365519039
NM_002290.4:c.5C>T