Allele Registry

Canonical Allele Identifier: PA181655

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000154900

RCV000201380

RCV000230724

RCV000621138

RCV000710279

ClinVar Variation:

178175

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Ile28017Val	CA181653 NM_001256850.1:c.84049A>G