Canonical Allele Identifier: PA311863
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Tyr5696His
CA311862
NM_001256850.1:c.17086T>C