Canonical Allele Identifier: PA2830224718
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asp23767His
CA349434738
NM_133432.3:c.71299G>C