Canonical Allele Identifier: PA2825552890
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 191678
ClinVar RCV Id: RCV000171966 RCV000692677 RCV000769186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098677.2:p.Gly1806Ser
CA237245
NM_001105207.3:c.5416G>A