Canonical Allele Identifier: PA2826417252
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg14556Cys
CA1994784
NM_001256850.1:c.43666C>T