Canonical Allele Identifier: PA311691
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203210

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Asp5226His
CA311689
NM_133379.5:c.15676G>C