Canonical Allele Identifier: PA2830223633
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asn22250Lys
CA1987281
NM_133432.3:c.66750T>A
CA349482231
NM_133432.3:c.66750T>G