Canonical Allele Identifier: PA2826417824
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 501556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro15597Ser
CA1994134
NM_001256850.1:c.46789C>T