Canonical Allele Identifier: PA2829429928
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46913

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val999Met
CA139502
NM_003319.4:c.2995G>A