Canonical Allele Identifier: PA282801
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46681
ClinVar RCV Id: RCV000039951 RCV000204819 RCV000245217 RCV000261603 RCV000316047 RCV000369529 RCV000319084 RCV000354529 RCV000770083 RCV001082805
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp6719Asn
CA282798
NM_001256850.1:c.20155G>A