Canonical Allele Identifier: PA2826421855
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467458

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly22865Asp
CA1990358
NM_001256850.1:c.68594G>A