Canonical Allele Identifier: PA2826426701
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp31066His
CA349434738
NM_001256850.1:c.93196G>C