Canonical Allele Identifier: PA1139758462
Gene: CABP4 HGNC NCBI
ClinVar RCV:
RCV001208017
ClinVar Variation:
938739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660201.1:p.His99Leu
CA381527553
NM_145200.5:c.296A>T