Canonical Allele Identifier: PA658664746
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn5314Asp
CA2002128
NM_001267550.2:c.15940A>G