Canonical Allele Identifier: PA645409149
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 283979

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala7230Val
CA2000967
NM_001267550.2:c.21689C>T