Canonical Allele Identifier: PA645408807
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val4350Met
CA2002633
NM_001267550.2:c.13048G>A