ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA141497
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
47609
ClinVar RCV Id:
RCV000040878
RCV000864110
RCV001132222
RCV001132224
RCV001132221
RCV001132223
RCV001132220
RCV001561054
RCV003486614
RCV004541194
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001254479.2:p.Lys32937Glu
CA141494
NM_001267550.2:c.98809A>G