Canonical Allele Identifier: PA2830202086
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 284493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn28999Ser
CA10604814
NM_133378.4:c.86996A>G