Canonical Allele Identifier: PA311108
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu33483Gln
CA311106
NM_001267550.2:c.100447G>C