Canonical Allele Identifier: PA2573254801
Gene: CNTNAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1515839
ClinVar RCV Id: RCV002023492
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054860.1:p.Thr427Ser
CA168690909
NM_014141.6:c.1280C>G
CA369924866
NM_014141.6:c.1279A>T