Canonical Allele Identifier: PA645409981
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro16243Thr
CA1994759
NM_001267550.2:c.48727C>A