Canonical Allele Identifier: PA2830238324
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ile19795Val
CA310728
NM_133437.4:c.59383A>G