Canonical Allele Identifier: PA2830233497
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 516827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asn11827Asp
CA1992270
NM_133437.4:c.35479A>G