Canonical Allele Identifier: PA139819
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47034
ClinVar RCV Id: RCV000040304 RCV000232832 RCV000618058 RCV001132983 RCV001132985 RCV001132984 RCV001136418 RCV001136419 RCV001170659 RCV001537833
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser1400Thr
CA139816
NM_001256850.1:c.4199G>C