Canonical Allele Identifier: PA2826421172
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191907

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala21707Thr
CA237839
NM_001256850.1:c.65119G>A