Canonical Allele Identifier: PA232529
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 137831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg3388Gln
CA232527
NM_001256850.1:c.10163G>A