Allele Registry

Canonical Allele Identifier: PA916066031

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000525649

ClinVar Variation:

467208

HGVS (amino-acid)	Matching Registered Transcripts
NP_597681.4:p.Pro7415Ser	CA60987700 NM_133437.4:c.22243C>T