Canonical Allele Identifier: PA2825552909
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1789258
ClinVar RCV Id: RCV002446302 RCV002463209 RCV003098792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098678.1:p.Arg8Cys
CA3966355
NM_001105208.3:c.22C>T