Canonical Allele Identifier: PA309702
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202595
ClinVar RCV Id: RCV000184479 RCV000226174
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val12721Leu
CA309701
NM_001267550.2:c.38161G>T
CA349476643
NM_001267550.2:c.38161G>C