Canonical Allele Identifier: PA2826415963
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178220
ClinVar RCV Id: RCV000154955 RCV000252544 RCV000467649 RCV001135957 RCV001134532 RCV001135955 RCV001135956 RCV001135958 RCV001697149 RCV001798508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys12017Arg
CA181823
NM_001256850.1:c.36050A>G