Canonical Allele Identifier: PA916017087
Gene: TTC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 314804
ClinVar RCV Id: RCV000300734 RCV000353073 RCV001094375 RCV001820932 RCV003888732 RCV003969880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275710.1:p.Ala504Val
CA7302781
NM_001288781.1:c.1511C>T