Canonical Allele Identifier: PA2828135288
Gene: LIFR HGNC NCBI

Linked Data

ClinVar Variation Id: 2149151
ClinVar RCV Id: RCV003065338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351226.1:p.Ala1026Val
CA3242512
NM_001364297.2:c.3077C>T