Canonical Allele Identifier: PA2825653387
Gene: LIFR HGNC NCBI

Linked Data

ClinVar Variation Id: 353622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121143.1:p.Met639Leu
CA3242807
NM_001127671.2:c.1915A>T
CA359539317
NM_001127671.2:c.1915A>C