Canonical Allele Identifier: PA2826414603
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405011

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu9050Phe
CA1999658
NM_001256850.1:c.27148C>T