Canonical Allele Identifier: PA2499265180
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1019594
ClinVar RCV Id: RCV001319050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala166_Ala167dup
CA2497074311
NM_003924.4:c.496_501dup
CA2670427177
NM_003924.4:c.486_491dup