ClinGen Allele Registry
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Canonical Allele Identifier:
PA2829436957
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
467400
ClinVar RCV Id:
RCV000532135
RCV001131635
RCV001131637
RCV001131639
RCV001584289
RCV001131636
RCV001131638
RCV001170576
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003310.4:p.Val13339Met
CA1991353
NM_003319.4:c.40015G>A