Canonical Allele Identifier: PA2825168750
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2076269
ClinVar RCV Id: RCV002979190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Gln2415His
CA365621967
NM_000426.4:c.7245A>C
CA365621970
NM_000426.4:c.7245A>T