Canonical Allele Identifier: PA2825166504
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 579145
ClinVar RCV Id: RCV000702355 RCV003130014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Leu51Phe
CA3992235
NM_000426.4:c.151C>T