Canonical Allele Identifier: PA2825028433
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 1499842
ClinVar RCV Id: RCV002042436
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000039.2:p.Met230Ile
CA367644657
NM_000048.4:c.690G>A
CA367644660
NM_000048.4:c.690G>C
CA367644662
NM_000048.4:c.690G>T