Canonical Allele Identifier: PA1139716327
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 855038
ClinVar RCV Id: RCV001060206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Ser841Arg
CA74481057
NM_002292.4:c.2521A>C
CA352720658
NM_002292.4:c.2523T>G
CA352720659
NM_002292.4:c.2523T>A