Allele Registry

Canonical Allele Identifier: PA309933

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000184573

ClinVar Variation:

202670

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Pro14615Thr	CA309932 NM_001256850.1:c.43843C>A