ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA141669
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
47669
ClinVar RCV Id:
RCV000040938
RCV000291584
RCV000344090
RCV000292859
RCV000350073
RCV000388022
RCV000474765
RCV000618932
RCV001703917
RCV004537120
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001254479.2:p.Glu34789Lys
CA141665
NM_001267550.2:c.104365G>A