Canonical Allele Identifier: PA2825659822
Gene: LAMA3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3117479
ClinVar RCV Id: RCV004407311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121190.2:p.Ala20Val
CA402044595
NM_001127718.2:c.59C>T