Canonical Allele Identifier: PA2825551676
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 999036
ClinVar RCV Id: RCV001294978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098677.2:p.Ala31Val
CA3966338
NM_001105207.3:c.92C>T