Canonical Allele Identifier: PA2826419102
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile17973Thr
CA1992767
NM_001256850.1:c.53918T>C