Canonical Allele Identifier: PA2580413093
Gene: TTC19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2109652
ClinVar RCV Id: RCV003038473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060245.3:p.Phe2Val
CA398381813
NM_017775.4:c.4T>G