Canonical Allele Identifier: PA658817246
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 534977
ClinVar RCV Id: RCV000642721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu34789Gln
CA349411899
NM_001267550.2:c.104365G>C