Canonical Allele Identifier: PA2826415627
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467052

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro11397Leu
CA1997854
NM_001256850.1:c.34190C>T