Canonical Allele Identifier: PA102618
Gene: HGD HGNC NCBI
ClinVar RCV:
RCV000003325
ClinVar Variation:
3175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000178.2:p.Gly270Arg
CA340049
NM_000187.4:c.808G>A
CA354074007
NM_000187.4:c.808G>C