Canonical Allele Identifier: PA311297
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203117
ClinVar RCV Id: RCV000534043 RCV000734760 RCV002408824
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser35839Arg
CA311295
NM_001267550.2:c.107517T>G
CA349400210
NM_001267550.2:c.107517T>A
CA349400215
NM_001267550.2:c.107515A>C