Canonical Allele Identifier: PA2825553009
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721572
ClinVar RCV Id: RCV002300529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098679.1:p.Asp35His
CA365518838
NM_001105209.3:c.103G>C