Canonical Allele Identifier: PA2826422268
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332777

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro23687Leu
CA1989973
NM_001256850.1:c.71060C>T