Canonical Allele Identifier: PA2826416761
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg13577Trp
CA1995385
NM_001256850.1:c.40729C>T