Canonical Allele Identifier: PA138893
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46663
ClinVar RCV Id: RCV000039933 RCV000643024 RCV001703895
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp6338Asn
CA138890
NM_001256850.1:c.19012G>A