Canonical Allele Identifier: PA2826415676
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro11501Ser
CA139513
NM_001256850.1:c.34501C>T