Canonical Allele Identifier: PA2828135307
Gene: LIFR HGNC NCBI

Linked Data

ClinVar Variation Id: 2150048
ClinVar RCV Id: RCV003083326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351226.1:p.Ser1056Pro
CA3242491
NM_001364297.2:c.3166T>C