Canonical Allele Identifier: PA178655
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165946
ClinVar RCV Id: RCV000152274 RCV000172300 RCV000306594 RCV000314770 RCV000366954 RCV000621257 RCV000363653 RCV000399359 RCV001170367 RCV001083650 RCV004532696
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg19409His
CA178653
NM_001267550.2:c.58226G>A