Canonical Allele Identifier: PA2830235414
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr14896Ser
CA1990648
NM_133437.4:c.44687C>G
CA1990651
NM_133437.4:c.44686A>T