Canonical Allele Identifier: PA2830214293
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180019
ClinVar RCV Id: RCV000156822 RCV000338432 RCV000279104 RCV000406384 RCV000407419 RCV000312780 RCV000714039 RCV001087961 RCV001798523 RCV004544459
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr6676Met
CA185646
NM_133432.3:c.20027C>T