Canonical Allele Identifier: PA2829435879
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 516827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asn11635Asp
CA1992270
NM_003319.4:c.34903A>G