Canonical Allele Identifier: PA2827588032
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004212269
ClinVar Variation:
2371430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338036.1:p.Thr540Asn
CA2393068
NM_001351107.2:c.1619C>A