Canonical Allele Identifier: PA352675
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 1901767
ClinVar RCV Id: RCV002577216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.Leu189Phe
CA352673
NM_000169.3:c.567G>C
CA413927813
NM_000169.3:c.567G>T