Canonical Allele Identifier: PA645409478
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404651

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro10586Leu
CA1998861
NM_001267550.2:c.31757C>T