Canonical Allele Identifier: PA2826515395
Gene: TTC19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1897506
ClinVar RCV Id: RCV002572076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258349.1:p.Leu267Phe
CA398379518
NM_001271420.2:c.801G>C
CA398379520
NM_001271420.2:c.801G>T