Canonical Allele Identifier: PA2830214592
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala7213Ser
CA10576523
NM_133432.3:c.21637G>T