Canonical Allele Identifier: PA2830240398
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala22911Val
CA349462688
NM_133437.4:c.68732C>T