Canonical Allele Identifier: PA2829442784
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala22719Val
CA349462688
NM_003319.4:c.68156C>T