Canonical Allele Identifier: PA181910
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178248

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Tyr6022Cys
CA181908
NM_001256850.1:c.18065A>G