Canonical Allele Identifier: PA104626
Gene: GALE HGNC NCBI

Linked Data

ClinVar Variation Id: 21172
ClinVar RCV Id: RCV000020294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000394.2:p.Arg239Trp
CA341699
NM_000403.4:c.715C>T