Canonical Allele Identifier: PA302889
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196066
ClinVar RCV Id: RCV000259190 RCV000539580 RCV000769926 RCV000724797 RCV002345607
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro27158Ala
CA302886
NM_001267550.2:c.81472C>G