Canonical Allele Identifier: PA2830232820
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ser10594Thr
CA60971692
NM_133437.4:c.31780T>A