ClinGen Allele Registry
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Canonical Allele Identifier:
PA181743
Gene: TTN
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000154926
RCV000172272
RCV000234385
RCV000248442
RCV000261085
RCV000262197
RCV000316255
RCV000370118
RCV000375502
ClinVar Variation:
178196
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001243779.1:p.Glu21172Lys
CA181741
NM_001256850.1:c.63514G>A