Canonical Allele Identifier: PA2830219700
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47328

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asn15903Asp
CA140696
NM_133432.3:c.47707A>G