Canonical Allele Identifier: PA2573223323
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1436377
ClinVar RCV Id: RCV001974745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Met1384Leu
CA352695860
NM_002292.4:c.4150A>T
CA352695864
NM_002292.4:c.4150A>C