Canonical Allele Identifier: PA915957158
Gene: ASL HGNC NCBI
ClinVar RCV:
RCV000674567
ClinVar Variation:
203612
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020117.1:p.Trp169Cys
CA312321
NM_001024946.2:c.507G>C
CA367642101
NM_001024946.2:c.507G>T