Canonical Allele Identifier: PA2826890336
Gene: SLMAP HGNC NCBI

Linked Data

ClinVar Variation Id: 532076
ClinVar RCV Id: RCV000638677 RCV003488749 RCV004025521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291349.1:p.Arg136Gln
CA2466795
NM_001304420.3:c.407G>A