Canonical Allele Identifier: PA2825168736
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 906087
ClinVar RCV Id: RCV001155017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Gly2396Arg
CA365621477
NM_000426.4:c.7186G>A
CA365621487
NM_000426.4:c.7186G>C