Canonical Allele Identifier: PA2826429077
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1014960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr33803Ala
CA349406047
NM_001256850.1:c.101407A>G