Canonical Allele Identifier: PA2829435426
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Pro10797Leu
CA283515
NM_003319.4:c.32390C>T