Canonical Allele Identifier: PA2830201351
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 499307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu27352Asp
CA1987872
NM_133378.4:c.82056A>C
CA349516193
NM_133378.4:c.82056A>T