Canonical Allele Identifier: PA310056
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202711

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg16424Cys
CA310055
NM_001256850.1:c.49270C>T