ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2829445241
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
282653
ClinVar RCV Id:
RCV000277595
RCV000525933
RCV001170288
RCV001293057
RCV001293174
RCV001572757
RCV001840468
RCV001840469
RCV001840470
RCV001840471
RCV004543009
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003310.4:p.Leu25718Phe
CA1985436
NM_003319.4:c.77152C>T