Canonical Allele Identifier: PA2825659542
Gene: LAMA3 HGNC NCBI
ClinVar RCV:
RCV002197374
ClinVar Variation:
1557840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121189.2:p.Gly2778Ser
CA297124538
NM_001127717.2:c.8332G>A