Canonical Allele Identifier: PA238074
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192002

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr9421Met
CA238072
NM_001267550.2:c.28262C>T