Canonical Allele Identifier: PA2830220789
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96306
ClinVar RCV Id: RCV000152208 RCV000261192 RCV000332574 RCV000389361 RCV000301222 RCV000467146 RCV000353634 RCV000723763 RCV001170790 RCV004529866 RCV002345399
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Phe17815Leu
CA178482
NM_133432.3:c.53443T>C
CA349589806
NM_133432.3:c.53445C>G
CA349589807
NM_133432.3:c.53445C>A