Canonical Allele Identifier: PA915967244
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 129438
ClinVar RCV Id: RCV000117445 RCV000390585 RCV000528731 RCV002490799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Thr1205Ala
CA153439
NM_001079823.2:c.3613A>G