Canonical Allele Identifier: PA282765
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46661
ClinVar RCV Id: RCV000039931 RCV000228030 RCV000294624 RCV000291004 RCV000315973 RCV000385353 RCV000349495 RCV000769059
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro5336Ser
CA282763
NM_133378.4:c.16006C>T