Canonical Allele Identifier: PA2830202017
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 506669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg28860Gly
CA1987153
NM_133378.4:c.86578C>G