Canonical Allele Identifier: PA2830243480
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2946668
ClinVar RCV Id: RCV003808906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Glu26491Asp
CA349407049
NM_133437.4:c.79473A>T
CA349407050
NM_133437.4:c.79473A>C