Canonical Allele Identifier: PA645381348
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Pro7855Ala
CA1994319
NM_003319.4:c.23563C>G