Allele Registry

Canonical Allele Identifier: PA138836

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000039912

RCV000545466

RCV000725041

ClinVar Variation:

46642

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Glu5904Asp	CA138833 NM_001256850.1:c.17712A>C CA349560408 NM_001256850.1:c.17712A>T