Canonical Allele Identifier: PA915982198
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 501044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu9802Gln
CA1999190
NM_001256850.1:c.29404G>C