Canonical Allele Identifier: PA2830210900
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166318

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Met1511Ile
CA179317
NM_133432.3:c.4533G>A
CA349462827
NM_133432.3:c.4533G>C
CA349462829
NM_133432.3:c.4533G>T