Canonical Allele Identifier: PA891852072
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 568845
ClinVar RCV Id: RCV000689328 RCV001024320
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala187Asp
CA356738065
NM_003924.4:c.560C>A