Canonical Allele Identifier: PA2573254743
Gene: BLNK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037446.1:p.Asp438Gly
CA377715094
NM_013314.4:c.1313A>G