Canonical Allele Identifier: PA645409445
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala9773Thr
CA1999409
NM_001267550.2:c.29317G>A