Canonical Allele Identifier: PA2829431306
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166292

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Pro3257Leu
CA179191
NM_003319.4:c.9770C>T