Canonical Allele Identifier: PA2830203991
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2038466
ClinVar RCV Id: RCV002907628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu32229Ala
CA60956253
NM_133378.4:c.96686A>C