Canonical Allele Identifier: PA2830202345
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 598666
ClinVar RCV Id: RCV000735115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp29450Glu
CA60970431
NM_133378.4:c.88350T>G
CA349454209
NM_133378.4:c.88350T>A