Canonical Allele Identifier: PA2830217028
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asn11501Ser
CA140219
NM_133432.3:c.34502A>G