Canonical Allele Identifier: PA2826419741
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467349

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Tyr19215Cys
CA1992209
NM_001256850.1:c.57644A>G