Canonical Allele Identifier: PA2825551647
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2978442
ClinVar RCV Id: RCV003837104 RCV004366887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098677.2:p.Trp7Leu
CA365519008
NM_001105207.3:c.20G>T