Canonical Allele Identifier: PA2825552811
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1429627
ClinVar RCV Id: RCV001967300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098677.2:p.Gly1681Ser
CA3964829
NM_001105207.3:c.5041G>A