Canonical Allele Identifier: PA2826426315
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala30455Thr
CA141378
NM_001256850.1:c.91363G>A