Canonical Allele Identifier: PA2573168394
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1509454
ClinVar RCV Id: RCV002017915
ClinVar Variation Id: 2895148
ClinVar RCV Id: RCV003739552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Lys2851Asn
CA3994863
NM_000426.4:c.8553G>T
CA365634719
NM_000426.4:c.8553G>C