Canonical Allele Identifier: PA2830192401
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala4940Thr
CA311880
NM_133378.4:c.14818G>A