Canonical Allele Identifier: PA2826422074
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu23313Phe
CA1990134
NM_001256850.1:c.69937C>T