ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA139532
Gene: TTN
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000040194
RCV000228887
RCV000725460
RCV001798148
ClinVar Variation:
46924
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_596869.4:p.Glu10667Lys
CA139530
NM_133378.4:c.31999G>A