Canonical Allele Identifier: PA2826418012
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282638

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gln15968Leu
CA1993920
NM_001256850.1:c.47903A>T