Canonical Allele Identifier: PA138947
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46683
ClinVar RCV Id: RCV000039953 RCV000082370 RCV000278937 RCV000275531 RCV000389765 RCV000333001 RCV000367843 RCV001079235 RCV001170083
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala5878Thr
CA138945
NM_133378.4:c.17632G>A