Canonical Allele Identifier: PA2741957801
Gene: PHIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2776234
ClinVar RCV Id: RCV003663063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060404.4:p.Phe1756Leu
CA364632806
NM_017934.7:c.5268T>G
CA364632810
NM_017934.7:c.5268T>A
CA364632825
NM_017934.7:c.5266T>C