Canonical Allele Identifier: PA2827365098
Gene: SRGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 208456
ClinVar RCV Id: RCV000190471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333130.1:p.Gln149His
CA204459
NM_001346201.2:c.447A>C
CA385662856
NM_001346201.2:c.447A>T