Canonical Allele Identifier: PA2830239546
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala21675Val
CA183496
NM_133437.4:c.65024C>T