Canonical Allele Identifier: PA915997764
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 822462
ClinVar RCV Id: RCV001017840 RCV001860878
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ser282Cys
CA356737013
NM_003924.4:c.845C>G