Canonical Allele Identifier: PA2830191706
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263726

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn3171Ser
CA2004300
NM_133378.4:c.9512A>G