Canonical Allele Identifier: PA311198
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203086
ClinVar RCV Id: RCV001704939 RCV001852407
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser34932Arg
CA311196
NM_001267550.2:c.104796T>G
CA349410905
NM_001267550.2:c.104796T>A
CA349410910
NM_001267550.2:c.104794A>C