Canonical Allele Identifier: PA658813412
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val9143Phe
CA1999808
NM_001267550.2:c.27427G>T