Canonical Allele Identifier: PA2829445303
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1417886
ClinVar RCV Id: RCV001940287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg25770Ser
CA349411521
NM_003319.4:c.77310A>T
CA349411522
NM_003319.4:c.77310A>C