Canonical Allele Identifier: PA141455
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47591
ClinVar RCV Id: RCV000040860 RCV000277556 RCV000303221 RCV000308086 RCV000369817 RCV000393698 RCV000619770 RCV000861079 RCV001575156 RCV003149662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala30052Val
CA141453
NM_133378.4:c.90155C>T