Canonical Allele Identifier: PA2830212500
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166292

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Pro3257Leu
CA179191
NM_133432.3:c.9770C>T