Canonical Allele Identifier: PA311487
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203155
ClinVar RCV Id: RCV000538379 RCV002390484 RCV001704945
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile2586Met
CA311485
NM_001256850.1:c.7758A>G