Canonical Allele Identifier: PA141988
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47826
ClinVar RCV Id: RCV000041095 RCV000229415 RCV000619226 RCV000770112 RCV001528764 RCV001839804 RCV001839806 RCV001839805 RCV001839807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile4194Phe
CA141984
NM_001267550.2:c.12580A>T