Canonical Allele Identifier: PA645410039
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 283015

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala16757Thr
CA10604370
NM_001267550.2:c.50269G>A