Canonical Allele Identifier: PA2830226602
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2939853
ClinVar RCV Id: RCV003795019

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ser25904Phe
CA1985409
NM_133432.3:c.77711C>T