Canonical Allele Identifier: PA916064944
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 499001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Phe5271Ile
CA349654857
NM_133437.4:c.15811T>A