Canonical Allele Identifier: PA2580413102
Gene: TTC19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1713512
ClinVar RCV Id: RCV002295522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060245.3:p.Gln41His
CA398382485
NM_017775.4:c.123G>C
CA398382487
NM_017775.4:c.123G>T