Canonical Allele Identifier: PA256526
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 12658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser4780Asn
CA256521
NM_001267550.2:c.14339G>A