Canonical Allele Identifier: PA2830221564
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332752

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gly19003Arg
CA10611610
NM_133432.3:c.57007G>A
CA349564215
NM_133432.3:c.57007G>C