Canonical Allele Identifier: PA140929
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47412
ClinVar RCV Id: RCV000040682 RCV000184884 RCV000620912 RCV000768904 RCV001086569 RCV001135731 RCV001135727 RCV001135728 RCV001135729 RCV001135730 RCV004534933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly25856Arg
CA140926
NM_001256850.1:c.77566G>A
CA349573256
NM_001256850.1:c.77566G>C