Canonical Allele Identifier: PA2829137172
Gene: SMARCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 573705
ClinVar RCV Id: RCV001026396 RCV000695437 RCV001809760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001374212.1:p.Gly25del
CA404054069
NM_001387283.1:c.73G>T
CA891843856
NM_001387283.1:c.74_76del