Canonical Allele Identifier: PA658812307
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 535774
ClinVar RCV Id: RCV000643949 RCV000764534 RCV003380658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Pro284Arg
CA356736989
NM_003924.4:c.851C>G