Canonical Allele Identifier: PA2830227120
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2016721
ClinVar RCV Id: RCV002851719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr26401Ser
CA349407201
NM_133432.3:c.79202C>G
CA349407203
NM_133432.3:c.79201A>T