ClinGen Allele Registry
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Canonical Allele Identifier:
PA309598
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
202562
ClinVar RCV Id:
RCV000184436
RCV000729422
RCV001132780
RCV001132781
RCV001136174
RCV001136176
RCV001136175
RCV001170627
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001254479.2:p.Thr10481Ala
CA309596
NM_001267550.2:c.31441A>G