Canonical Allele Identifier: PA309976
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202684
ClinVar RCV Id: RCV000225833 RCV001130075 RCV001130077 RCV001130074 RCV001130076 RCV001135104 RCV002444751 RCV001704902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu16890Ala
CA309974
NM_001267550.2:c.50669A>C