Canonical Allele Identifier: PA141127
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47474
ClinVar RCV Id: RCV000040743 RCV000172214 RCV000245043 RCV001086668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Phe29395Leu
CA141123
NM_001267550.2:c.88183T>C
CA349530998
NM_001267550.2:c.88185C>G
CA349531001
NM_001267550.2:c.88185C>A