Canonical Allele Identifier: PA645411573
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405015

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met28214Val
CA1988755
NM_001267550.2:c.84640A>G