Canonical Allele Identifier: PA141125
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47474
ClinVar RCV Id: RCV000040743 RCV000172214 RCV000245043 RCV001086668
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Phe26827Leu
CA141123
NM_133378.4:c.80479T>C
CA349530998
NM_133378.4:c.80481C>G
CA349531001
NM_133378.4:c.80481C>A