Canonical Allele Identifier: PA2825167589
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 162576
ClinVar RCV Id: RCV000712184 RCV000764624 RCV000550298 RCV001156479 RCV001270116 RCV001252051 RCV004532672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Ala1178Thr
CA295392
NM_000426.4:c.3532G>A