Canonical Allele Identifier: PA1139713175
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 840364
ClinVar RCV Id: RCV001042332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ile280Val
CA356737040
NM_003924.4:c.838A>G