Canonical Allele Identifier: PA179311
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166316
ClinVar RCV Id: RCV000152502 RCV000252820 RCV000302656 RCV000404360 RCV000362079 RCV000308535 RCV000337667 RCV000471450 RCV003137662 RCV004532709
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Thr1733Met
CA179307
NM_133379.5:c.5198C>T