Canonical Allele Identifier: PA178777
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165992
ClinVar RCV Id: RCV000152326 RCV000250139 RCV000541819 RCV003137656
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala15103Val
CA178776
NM_133378.4:c.45308C>T