Canonical Allele Identifier: PA2829439505
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_003310.4:p.Phe17690Leu
CA178482
NM_003319.4:c.53068T>C
CA349589806
NM_003319.4:c.53070C>G
CA349589807
NM_003319.4:c.53070C>A