Canonical Allele Identifier: PA658806223
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Phe989Leu
CA2005674
NM_133379.5:c.2967C>A
CA349491103
NM_133379.5:c.2967C>G
CA349491153
NM_133379.5:c.2965T>C