Canonical Allele Identifier: PA2826416960
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47006
ClinVar RCV Id: RCV000040276 RCV000287419 RCV000272075 RCV000322491 RCV000342339 RCV000377170 RCV000470629 RCV000617450 RCV001719770 RCV004534900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala13986Val
CA139743
NM_001256850.1:c.41957C>T