Canonical Allele Identifier: PA2830242919
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1417886
ClinVar RCV Id: RCV001940287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg25962Ser
CA349411521
NM_133437.4:c.77886A>T
CA349411522
NM_133437.4:c.77886A>C