Canonical Allele Identifier: PA1139712436
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 959613
ClinVar RCV Id: RCV001232997 RCV003473801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala167Thr
CA356738504
NM_003924.4:c.499G>A