Canonical Allele Identifier: PA2830238222
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448822

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr19620Ala
CA60984661
NM_133437.4:c.58858A>G