Canonical Allele Identifier: PA2499283677
Gene: TTC19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1059427
ClinVar RCV Id: RCV001368703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060245.3:p.Pro38Thr
CA288187841
NM_017775.4:c.112C>A