ClinGen Allele Registry
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Canonical Allele Identifier:
PA916037832
Gene: PAH
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
108308
ClinVar RCV:
RCV000088808
RCV001269318
ClinVar Variation:
102572
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001341233.1:p.Phe410Cys
CA229406
NM_001354304.2:c.1229T>G