Canonical Allele Identifier: PA2830210732
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala1338Ser
CA2005396
NM_133432.3:c.4012G>T