Canonical Allele Identifier: PA2830199856
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly23948Ser
CA1989460
NM_133378.4:c.71842G>A