Canonical Allele Identifier: PA645410546
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 228120

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala21110Val
CA1992104
NM_001267550.2:c.63329C>T