Canonical Allele Identifier: PA915965041
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 162576
ClinVar RCV Id: RCV000712184 RCV000764624 RCV000550298 RCV001156479 RCV001270116 RCV001252051 RCV004532672
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Ala1178Thr
CA295392
NM_001079823.2:c.3532G>A