Canonical Allele Identifier: PA2826414222
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263481

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg8329His
CA2000097
NM_001256850.1:c.24986G>A