Canonical Allele Identifier: PA2830209244
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202971

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Tyr27737His
CA310849
NM_133378.4:c.83209T>C