Canonical Allele Identifier: PA2825699730
Gene: SMARCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1467973
ClinVar RCV Id: RCV001993535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122321.1:p.Thr1455Ser
CA404073393
NM_001128849.1:c.4363A>T
CA404073412
NM_001128849.1:c.4364C>G