Canonical Allele Identifier: PA645382851
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Glu1174Asp
CA2005539
NM_133379.5:c.3522A>C
CA349483110
NM_133379.5:c.3522A>T