ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA916037736
Gene: PAH
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
358086
ClinVar RCV:
RCV000410352
ClinVar Variation:
371278
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001341233.1:p.Phe331Ser
CA16020915
NM_001354304.2:c.992T>C