Canonical Allele Identifier: PA2499247951
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_001304853.1:p.Phe52Leu
CA356633814
NM_001317924.2:c.154T>C
CA356633823
NM_001317924.2:c.156T>G
CA356633825
NM_001317924.2:c.156T>A