Canonical Allele Identifier: PA915986634
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg9897Trp
CA60975146
NM_003319.4:c.29689C>T