Canonical Allele Identifier: PA2825094059
Gene: LAMA3 HGNC NCBI
ClinVar RCV:
RCV002197374
ClinVar Variation:
1557840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000218.3:p.Gly1225Ser
CA297124538
NM_000227.6:c.3673G>A