Canonical Allele Identifier: PA2829443015
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 598664
ClinVar RCV Id: RCV000735113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala23022Gly
CA349450843
NM_003319.4:c.69065C>G