Canonical Allele Identifier: PA915974214
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 643208
ClinVar RCV Id: RCV000796863 RCV002345760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098676.2:p.Asn1752Asp
CA144877274
NM_001105206.3:c.5254A>G