Canonical Allele Identifier: PA2826411222
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192073
ClinVar RCV Id: RCV000172464 RCV000642748 RCV002362887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn2309Lys
CA238249
NM_001256850.1:c.6927T>A
CA349681409
NM_001256850.1:c.6927T>G