Canonical Allele Identifier: PA2828135845
Gene: LIFR HGNC NCBI

Linked Data

ClinVar Variation Id: 2149151
ClinVar RCV Id: RCV003065338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351227.1:p.Ala1015Val
CA3242512
NM_001364298.2:c.3044C>T