Canonical Allele Identifier: PA658668518
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met34251Lys
CA1985710
NM_001267550.2:c.102752T>A