Canonical Allele Identifier: PA645412561
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404628
ClinVar RCV Id: RCV000471780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gln33340Lys
CA1986088
NM_001267550.2:c.100018C>A