Canonical Allele Identifier: PA2580176446
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1757065
ClinVar RCV Id: RCV002365156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu32697Asp
CA1986445
NM_001267550.2:c.98091A>C
CA349434898
NM_001267550.2:c.98091A>T