Canonical Allele Identifier: PA645410697
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332801

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro22258Ser
CA1991433
NM_001267550.2:c.66772C>T