Canonical Allele Identifier: PA2830225522
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Cys24896Ser
CA311127
NM_133432.3:c.74686T>A
CA349420561
NM_133432.3:c.74687G>C