ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA140298
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
47197
ClinVar RCV Id:
RCV000040467
RCV000082417
RCV000143969
RCV000262231
RCV000297845
RCV000312697
RCV000357132
RCV000393151
RCV000619500
RCV000852825
RCV001086280
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_596869.4:p.Ile18629Val
CA140295
NM_133378.4:c.55885A>G