Canonical Allele Identifier: PA140672
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47318
ClinVar RCV Id: RCV000040588 RCV000118779 RCV000249950 RCV000769952 RCV001083516 RCV001131595 RCV001131997 RCV001131999 RCV001131996 RCV001131998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr22670Ala
CA140669
NM_001256850.1:c.68008A>G