Canonical Allele Identifier: PA2826429093
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 586862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly33822Ala
CA1985112
NM_001256850.1:c.101465G>C