Canonical Allele Identifier: PA2830204022
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203081

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala32257Asp
CA311181
NM_133378.4:c.96770C>A