Canonical Allele Identifier: PA2829431266
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val3204Gly
CA141720
NM_003319.4:c.9611T>G