Canonical Allele Identifier: PA2830212427
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val3204Gly
CA141720
NM_133432.3:c.9611T>G