Canonical Allele Identifier: PA2829430138
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala1338Ser
CA2005396
NM_003319.4:c.4012G>T