Canonical Allele Identifier: PA2825551153
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2500664
ClinVar RCV Id: RCV003225576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098676.2:p.Pro33Ala
CA365518850
NM_001105206.3:c.97C>G