Canonical Allele Identifier: PA2741964145
Gene: TTC19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2606388
ClinVar RCV Id: RCV003352636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060245.3:p.Ser6Asn
CA398381884
NM_017775.4:c.17G>A