Canonical Allele Identifier: PA2573223096
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1516280
ClinVar RCV Id: RCV002023833
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Phe871Leu
CA2394267
NM_002292.4:c.2611T>C
CA352719325
NM_002292.4:c.2613C>G
CA352719333
NM_002292.4:c.2613C>A