Canonical Allele Identifier: PA2825552986
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2504904
ClinVar RCV Id: RCV003234495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098679.1:p.Ala19Val
CA3966350
NM_001105209.3:c.56C>T