Canonical Allele Identifier: PA645410909
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg24056Ser
CA10611620
NM_001267550.2:c.72166C>A