Canonical Allele Identifier: PA1139736107
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 969532
ClinVar RCV Id: RCV001244907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054859.2:p.Ala127Pro
CA2097586
NM_014140.4:c.379G>C