Canonical Allele Identifier: PA645426947
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 406411
ClinVar RCV Id: RCV000476224 RCV001026141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly240Asp
CA16611433
NM_003924.4:c.719G>A