Canonical Allele Identifier: PA139046
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46721
ClinVar RCV Id: RCV000039991 RCV000082372 RCV000293069 RCV000390050 RCV000335014 RCV000352590 RCV000406710 RCV000852891 RCV001082941 RCV001798135
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Phe7846Leu
CA139042
NM_001267550.2:c.23538C>G
CA349508808
NM_001267550.2:c.23538C>A
CA349508841
NM_001267550.2:c.23536T>C