Canonical Allele Identifier: PA2825551644
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2062170
ClinVar RCV Id: RCV002953231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098677.2:p.Ala2Val
CA365519039
NM_001105207.3:c.5C>T