Canonical Allele Identifier: PA2829436686
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg12931Cys
CA1991600
NM_003319.4:c.38791C>T