Canonical Allele Identifier: PA2825630320
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 392887
ClinVar RCV Id: RCV000431974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120679.1:p.Asp816Glu
CA16604060
NM_001127207.2:c.2448C>A
CA350504709
NM_001127207.2:c.2448C>G