Canonical Allele Identifier: PA2825167038
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 92941
ClinVar RCV Id: RCV000078750 RCV000555236 RCV001152471 RCV001729381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Gly600Arg
CA248661
NM_000426.4:c.1798G>A
CA365609490
NM_000426.4:c.1798G>C