Canonical Allele Identifier: PA2829443434
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asp23642His
CA349434738
NM_003319.4:c.70924G>C