Canonical Allele Identifier: PA2826428285
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala33031Val
CA1985501
NM_001256850.1:c.99092C>T