Canonical Allele Identifier: PA140417
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47238

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp20584Asn
CA140414
NM_001256850.1:c.61750G>A