Canonical Allele Identifier: PA2830209274
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val32739Ala
CA1985188
NM_133378.4:c.98216T>C