Canonical Allele Identifier: PA645411945
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr30218Ala
CA1987762
NM_001267550.2:c.90652A>G