Canonical Allele Identifier: PA645410136
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282638

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gln17609Leu
CA1993920
NM_001267550.2:c.52826A>T