ClinGen Allele Registry
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Canonical Allele Identifier:
PA916037654
Gene: PAH
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
15642
ClinVar RCV:
RCV000000634
RCV000078531
ClinVar Variation:
603
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001341233.1:p.Tyr277Asp
CA251534
NM_001354304.2:c.829T>G