Canonical Allele Identifier: PA2826414591
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu9035Ser
CA1999665
NM_001256850.1:c.27104T>C