Canonical Allele Identifier: PA2829441928
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala21483Val
CA183496
NM_003319.4:c.64448C>T