Canonical Allele Identifier: PA238256
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192074
ClinVar RCV Id: RCV000172465 RCV001078603
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr2257Ser
CA238254
NM_001267550.2:c.6770C>G
CA349682052
NM_001267550.2:c.6769A>T