Canonical Allele Identifier: PA309077
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202320

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val20732Asp
CA309076
NM_001256850.1:c.62195T>A