Canonical Allele Identifier: PA2830207397
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val17318Gly
CA310149
NM_133378.4:c.51953T>G