Canonical Allele Identifier: PA2580417682
Gene: PHIP HGNC NCBI
ClinVar RCV:
RCV002766672
ClinVar Variation:
1982278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060404.4:p.Val1647Ile
CA364633642
NM_017934.7:c.4939G>A