Canonical Allele Identifier: PA2830192077
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn4070Asp
CA2002128
NM_133378.4:c.12208A>G