Canonical Allele Identifier: PA2825660566
Gene: LAMA3 HGNC NCBI

Linked Data

ClinVar Variation Id: 768931
ClinVar RCV Id: RCV000947874 RCV002546015 RCV004543557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121190.2:p.Thr1527Ser
CA8917230
NM_001127718.2:c.4579A>T
CA402052007
NM_001127718.2:c.4580C>G