Canonical Allele Identifier: PA1139712398
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 946861
ClinVar RCV Id: RCV001217812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala159Val
CA356738644
NM_003924.4:c.476C>T