Canonical Allele Identifier: PA1139708624
Gene: HRC HGNC NCBI

Linked Data

ClinVar Variation Id: 369288
ClinVar RCV Id: RCV000397811
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002143.1:p.Asp261del
CA9568374
NM_002152.3:c.782_784del
CA645605432
NM_002152.3:c.782_783insATG