Canonical Allele Identifier: PA2830235466
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Gly14997Ser
CA178519
NM_133437.4:c.44989G>A