Canonical Allele Identifier: PA916066862
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val9356Met
CA139984
NM_133437.4:c.28066G>A