Canonical Allele Identifier: PA139764
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47013
ClinVar RCV Id: RCV000040283 RCV000082410 RCV000299345 RCV000314422 RCV000349511 RCV000369133 RCV000406274 RCV000619989 RCV000852853 RCV001083906 RCV001798153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro13281Thr
CA139762
NM_133378.4:c.39841C>A