Canonical Allele Identifier: PA2830230220
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47636
ClinVar RCV Id: RCV000040905 RCV000082466 RCV000247307 RCV000282222 RCV000286768 RCV000371851 RCV000317271 RCV000341793 RCV000852925 RCV001084199 RCV000769103 RCV004534955
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg3074Gln
CA141561
NM_133437.4:c.9221G>A