Canonical Allele Identifier: PA2826257337
Gene: ASB11 HGNC NCBI
ClinVar RCV:
RCV000964441
ClinVar Variation:
782970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001188512.1:p.Arg191Trp
CA10353850
NM_001201583.2:c.571A>T