Canonical Allele Identifier: PA2830215857
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Pro9420Leu
CA310086
NM_133432.3:c.28259C>T