Canonical Allele Identifier: PA311162
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg34637Trp
CA311160
NM_001267550.2:c.103909C>T