Canonical Allele Identifier: PA2826420810
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gln21058His
CA183247
NM_001256850.1:c.63174G>C
CA349421653
NM_001256850.1:c.63174G>T