Canonical Allele Identifier: PA2830215512
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 413198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Phe8814Ser
CA1993835
NM_133432.3:c.26441T>C