Canonical Allele Identifier: PA179224
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg3163His
CA179222
NM_001256850.1:c.9488G>A