Canonical Allele Identifier: PA2825552237
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 518371
ClinVar RCV Id: RCV000607294 RCV002448911 RCV001701393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098677.2:p.Phe762Leu
CA365383496
NM_001105207.3:c.2286T>G
CA365383497
NM_001105207.3:c.2286T>A
CA365383501
NM_001105207.3:c.2284T>C