Canonical Allele Identifier: PA2829435213
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202736
ClinVar RCV Id: RCV000184656
ClinVar Variation Id: 467313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asp10425Glu
CA310128
NM_003319.4:c.31275T>G
CA1992846
NM_003319.4:c.31275T>A