Canonical Allele Identifier: PA2573223347
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1512103
ClinVar RCV Id: RCV002017000
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Ala1487Val
CA352692668
NM_002292.4:c.4460C>T