Canonical Allele Identifier: PA2829442680
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Gly22630Arg
CA141322
NM_003319.4:c.67888G>A
CA349466615
NM_003319.4:c.67888G>C