Canonical Allele Identifier: PA140015
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47103
ClinVar RCV Id: RCV000040373 RCV000797680 RCV003156220
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Lys15855Asn
CA140013
NM_133378.4:c.47565G>C
CA349543218
NM_133378.4:c.47565G>T