Canonical Allele Identifier: PA185750
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile30627Val
CA185748
NM_001267550.2:c.91879A>G