Canonical Allele Identifier: PA2825454098
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 477510
ClinVar RCV Id: RCV000544403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Thr2577Ser
CA365628438
NM_001079823.2:c.7729A>T
CA365628442
NM_001079823.2:c.7730C>G