Canonical Allele Identifier: PA2829442963
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203019

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val22941Met
CA310995
NM_003319.4:c.68821G>A