Canonical Allele Identifier: PA312146
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203359
ClinVar RCV Id: RCV000554086 RCV000714005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr9261Met
CA312145
NM_001256850.1:c.27782C>T