Canonical Allele Identifier: PA2830230311
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val3204Gly
CA141720
NM_133437.4:c.9611T>G