Canonical Allele Identifier: PA2826415771
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro11623Leu
CA1996729
NM_001256850.1:c.34868C>T