Canonical Allele Identifier: PA2573247063
Gene: CRYGB HGNC NCBI
ClinVar RCV:
RCV001925904
ClinVar Variation:
1413387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005201.2:p.Pro84Leu
CA2078110
NM_005210.4:c.251C>T