Canonical Allele Identifier: PA2573223088
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1361204
ClinVar RCV Id: RCV001907409
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Ala838Val
CA352720792
NM_002292.4:c.2513C>T