Canonical Allele Identifier: PA916066267
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Gly8008Ala
CA1994330
NM_133437.4:c.24023G>C