Canonical Allele Identifier: PA181615
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96316
ClinVar RCV Id: RCV000082452 RCV000154888 RCV000263196 RCV000312560 RCV000317322 RCV000465970 RCV000355719 RCV000369634 RCV001170760 RCV002362734 RCV004529869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile30116Thr
CA181612
NM_001256850.1:c.90347T>C