Canonical Allele Identifier: PA2825338781
Gene: ASL HGNC NCBI

Linked Data

ClinVar Variation Id: 1499842
ClinVar RCV Id: RCV002042436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020117.1:p.Met204Ile
CA367644657
NM_001024946.2:c.612G>A
CA367644660
NM_001024946.2:c.612G>C
CA367644662
NM_001024946.2:c.612G>T