Canonical Allele Identifier: PA181664
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178176
ClinVar RCV Id: RCV000154902 RCV000464472 RCV001136032 RCV001136034 RCV001136033 RCV001136035 RCV001136036 RCV002354367 RCV004534968
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr27806Arg
CA181662
NM_001256850.1:c.83417C>G