Canonical Allele Identifier: PA645412808
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr35125Met
CA1985271
NM_001267550.2:c.105374C>T