Canonical Allele Identifier: PA237732
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191863

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile26861Val
CA237731
NM_133378.4:c.80581A>G