Canonical Allele Identifier: PA140657
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47314
ClinVar RCV Id: RCV000040584 RCV000558833 RCV001703906
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg24163His
CA140653
NM_001267550.2:c.72488G>A