Canonical Allele Identifier: PA2829434208
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala8606Val
CA178776
NM_003319.4:c.25817C>T