ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2830220925
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
179002
ClinVar RCV Id:
RCV000155780
RCV000172245
RCV000254311
RCV000291098
RCV000316713
RCV000330851
RCV000385420
RCV000371276
RCV001078567
RCV001170788
RCV001293186
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_597676.3:p.Thr18013Met
CA183467
NM_133432.3:c.54038C>T