Canonical Allele Identifier: PA2830192359
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg4814Cys
CA311868
NM_133378.4:c.14440C>T