Canonical Allele Identifier: PA139516
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46915
ClinVar RCV Id: RCV000040185 RCV000082395 RCV001083903 RCV000852867 RCV001136516 RCV001133068 RCV001133069 RCV001133070 RCV001133071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro12478Ser
CA139513
NM_001267550.2:c.37432C>T