Canonical Allele Identifier: PA141668
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu33148Lys
CA141665
NM_001256850.1:c.99442G>A