Canonical Allele Identifier: PA237856
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu19873Gly
CA237855
NM_133378.4:c.59618A>G