Canonical Allele Identifier: PA2830214179
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467172
ClinVar RCV Id: RCV000531429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Pro6450Leu
CA60993148
NM_133432.3:c.19349C>T