Canonical Allele Identifier: PA141608
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47651
ClinVar RCV Id: RCV000040920 RCV001088345 RCV000786253 RCV002371852 RCV004534956
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Arg3163Cys
CA141602
NM_133379.5:c.9487C>T