Canonical Allele Identifier: PA179309
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166316
ClinVar RCV Id: RCV000152502 RCV000252820 RCV000302656 RCV000404360 RCV000362079 RCV000308535 RCV000337667 RCV000471450 RCV003137662 RCV004532709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr1733Met
CA179307
NM_001267550.2:c.5198C>T