Canonical Allele Identifier: PA2830222330
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr20264Arg
CA310756
NM_133432.3:c.60791C>G