Canonical Allele Identifier: PA2826422301
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Tyr23734Phe
CA178498
NM_001256850.1:c.71201A>T