Canonical Allele Identifier: PA2830239339
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Pro21358Ser
CA1987758
NM_133437.4:c.64072C>T