Canonical Allele Identifier: PA1139691431
Gene: TFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 990095
ClinVar RCV Id: RCV001278037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193784.1:p.Asp59Glu
CA4386752
NM_001206855.3:c.177C>G
CA368534287
NM_001206855.3:c.177C>A