Canonical Allele Identifier: PA2826421541
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile22319Thr
CA1990576
NM_001256850.1:c.66956T>C