Canonical Allele Identifier: PA658817250
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535257
ClinVar RCV Id: RCV000643126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu34790Phe
CA1985433
NM_001267550.2:c.104368C>T