Canonical Allele Identifier: PA2826425114
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro28590Ser
CA1987758
NM_001256850.1:c.85768C>T