Canonical Allele Identifier: PA140252
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47184
ClinVar RCV Id: RCV000040454 RCV000172728 RCV000329243 RCV000617741 RCV000852935 RCV001086722 RCV001798169 RCV004528211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala1827Ser
CA140248
NM_001267550.2:c.5479G>T