ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA209319
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
212484
ClinVar RCV Id:
RCV000194864
RCV000643786
RCV000727832
RCV001798661
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_596869.4:p.Pro30626Leu
CA209318
NM_133378.4:c.91877C>T