Canonical Allele Identifier: PA2829434645
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr9395Ala
CA178711
NM_003319.4:c.28183A>G