Canonical Allele Identifier: PA309720
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202602
ClinVar RCV Id: RCV000643813 RCV000725487
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val13084Leu
CA309718
NM_001267550.2:c.39250G>T
CA1996801
NM_001267550.2:c.39250G>C