ClinGen Allele Registry
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Canonical Allele Identifier:
PA181650
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000154899
RCV000618633
RCV000727232
RCV000769893
RCV001079791
ClinVar Variation:
178174
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_596869.4:p.Gly27094Ser
CA181649
NM_133378.4:c.81280G>A