Canonical Allele Identifier: PA2826515331
Gene: TTC19 HGNC NCBI

Linked Data

ClinVar Variation Id: 3184142
ClinVar RCV Id: RCV004479028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258349.1:p.Ile99Met
CA8407469
NM_001271420.2:c.297T>G