Canonical Allele Identifier: PA2741957781
Gene: PHIP HGNC NCBI
ClinVar RCV:
RCV003873837
ClinVar Variation:
3015750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060404.4:p.Gly1629Arg
CA3899337
NM_017934.7:c.4885G>A
CA364633759
NM_017934.7:c.4885G>C