Canonical Allele Identifier: PA2830238008
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asn19260Ser
CA184934
NM_133437.4:c.57779A>G