Canonical Allele Identifier: PA2825579422
Gene: SH2D1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2138714
ClinVar RCV Id: RCV003041478 RCV003236948
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108409.1:p.Ser34Arg
CA414122377
NM_001114937.3:c.100A>C
CA414122383
NM_001114937.3:c.102C>A
CA414122384
NM_001114937.3:c.102C>G