Canonical Allele Identifier: PA1139712952
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 935491
ClinVar RCV Id: RCV001204093 RCV002379774 RCV003324820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala242Val
CA356737255
NM_003924.4:c.725C>T