Canonical Allele Identifier: PA2830203168
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg31170His
CA311124
NM_133378.4:c.93509G>A