ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA282637
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
46578
ClinVar RCV Id:
RCV000039848
RCV000205174
RCV000249819
RCV001134669
RCV001134671
RCV001134673
RCV001528575
RCV001134670
RCV001134672
RCV003486570
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_596869.4:p.Arg3367Gln
CA282632
NM_133378.4:c.10100G>A