Canonical Allele Identifier: PA2826422392
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val23926Phe
CA1989872
NM_001256850.1:c.71776G>T