Canonical Allele Identifier: PA645383877
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Ile3116Met
CA2004349
NM_133379.5:c.9348C>G