Canonical Allele Identifier: PA2830232830
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_597681.4:p.Asp10617Glu
CA310128
NM_133437.4:c.31851T>G
CA1992846
NM_133437.4:c.31851T>A