Canonical Allele Identifier: PA2826413684
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro7226Leu
CA2000798
NM_001256850.1:c.21677C>T