Canonical Allele Identifier: PA2830054147
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1022134
ClinVar RCV Id: RCV001322005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Phe212Leu
CA356633814
NM_025132.4:c.634T>C
CA356633823
NM_025132.4:c.636T>G
CA356633825
NM_025132.4:c.636T>A