Canonical Allele Identifier: PA915986652
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile9959Val
CA10576512
NM_003319.4:c.29875A>G