Canonical Allele Identifier: PA645381378
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro8833Leu
CA1999202
NM_133378.4:c.26498C>T