Canonical Allele Identifier: PA181878
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178236
ClinVar RCV Id: RCV000154973 RCV000287568 RCV000326198 RCV000327268 RCV000384268 RCV000387819 RCV000725482 RCV001084561
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg7672Cys
CA181876
NM_001256850.1:c.23014C>T