Canonical Allele Identifier: PA2828135316
Gene: LIFR HGNC NCBI

Linked Data

ClinVar Variation Id: 618197
ClinVar RCV Id: RCV000756307 RCV001151740 RCV002533786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351226.1:p.Asp1074Gly
CA3242485
NM_001364297.2:c.3221A>G