Canonical Allele Identifier: PA2829435151
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr10332Met
CA178656
NM_003319.4:c.30995C>T