Canonical Allele Identifier: PA289127
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47674
ClinVar RCV Id: RCV000040943 RCV000118804 RCV000250530 RCV000768826 RCV001135062 RCV001135064 RCV001080684 RCV001135063 RCV001135065 RCV001135061 RCV004528225
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val34854Leu
CA289122
NM_001267550.2:c.104560G>C
CA349411400
NM_001267550.2:c.104560G>T