Canonical Allele Identifier: PA658664409
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 486036
ClinVar RCV Id: RCV000572360 RCV000707232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly170Arg
CA2901484
NM_003924.4:c.508G>C