Canonical Allele Identifier: PA2826411981
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala3744Thr
CA141976
NM_001256850.1:c.11230G>A