Canonical Allele Identifier: PA916066895
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ile9507Thr
CA140004
NM_133437.4:c.28520T>C