Allele Registry

Canonical Allele Identifier: PA140056

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000040387

RCV000768980

RCV001130203

RCV001130204

RCV001130205

RCV001130206

RCV001130207

RCV001703902

RCV002433518

ClinVar Variation:

47117

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Ala17340Val	CA140053 NM_001256850.1:c.52019C>T