Canonical Allele Identifier: PA2826418978
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr17756Met
CA178656
NM_001256850.1:c.53267C>T