Canonical Allele Identifier: PA2826420319
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535329

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala20215Thr
CA1991684
NM_001256850.1:c.60643G>A