Canonical Allele Identifier: PA231602
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly19750Ser
CA231599
NM_001267550.2:c.59248G>A