Canonical Allele Identifier: PA2826424161
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile27027Thr
CA181672
NM_001256850.1:c.81080T>C