Canonical Allele Identifier: PA915989166
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 805710
ClinVar RCV Id: RCV000993414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile9389Val
CA349439902
NM_001267550.2:c.28165A>G