Canonical Allele Identifier: PA312122
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser8920Ala
CA312121
NM_001256850.1:c.26758T>G