Canonical Allele Identifier: PA2830224213
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1755861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val23019Leu
CA349456531
NM_133432.3:c.69055G>T
CA349456533
NM_133432.3:c.69055G>C