Canonical Allele Identifier: PA2830241050
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asp23834His
CA349434738
NM_133437.4:c.71500G>C