Canonical Allele Identifier: PA140580
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47286
ClinVar RCV Id: RCV000040556 RCV000184775 RCV000544602 RCV001130762 RCV001130763 RCV001130764 RCV001133729 RCV001133730 RCV002326752
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly20930Ser
CA140578
NM_133378.4:c.62788G>A