Canonical Allele Identifier: PA1139687117
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 846158
ClinVar RCV Id: RCV001049395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu35384Lys
CA349406911
NM_001267550.2:c.106150G>A