Canonical Allele Identifier: PA1139687079
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 959891
ClinVar RCV Id: RCV001233323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser35368Pro
CA349407031
NM_001267550.2:c.106102T>C