Canonical Allele Identifier: PA916066939
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg9600Gly
CA310095
NM_133437.4:c.28798A>G