Canonical Allele Identifier: PA2826412345
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 12658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser4463Asn
CA256521
NM_001256850.1:c.13388G>A