Canonical Allele Identifier: PA2830236475
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val16778Ala
CA310557
NM_133437.4:c.50333T>C