Canonical Allele Identifier: PA140435
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47243
ClinVar RCV Id: RCV000040513 RCV000266781 RCV000269962 RCV000323852 RCV000384336 RCV000617644 RCV000327353 RCV000456180 RCV001703904
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val19732Ile
CA140433
NM_133378.4:c.59194G>A