Canonical Allele Identifier: PA2741903986
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2831033
ClinVar RCV Id: RCV003634936 RCV004371743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ser171Phe
CA356738419
NM_003924.4:c.512C>T