Canonical Allele Identifier: PA916064759
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val4957Ile
CA309778
NM_133437.4:c.14869G>A