Canonical Allele Identifier: PA2829442962
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 808911
ClinVar RCV Id: RCV000997347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val22941Ala
CA60970498
NM_003319.4:c.68822T>C