Canonical Allele Identifier: PA311814
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203250

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn5337Ser
CA311812
NM_001267550.2:c.16010A>G