Canonical Allele Identifier: PA2829442927
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1755861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val22894Leu
CA349456531
NM_003319.4:c.68680G>T
CA349456533
NM_003319.4:c.68680G>C