Canonical Allele Identifier: PA645508580
Gene: PROB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 225701
ClinVar RCV Id: RCV000491696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155018.1:p.Gly224Asp
CA361161282
NM_001161546.1:c.671G>A