Canonical Allele Identifier: PA2829440280
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332752

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Gly18878Arg
CA10611610
NM_003319.4:c.56632G>A
CA349564215
NM_003319.4:c.56632G>C