Canonical Allele Identifier: PA2826420564
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu20619Gln
CA1991432
NM_001256850.1:c.61855G>C