Canonical Allele Identifier: PA126995
Gene: CRYM HGNC NCBI

Linked Data

ClinVar Variation Id: 16935
ClinVar RCV Id: RCV000018443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001879.1:p.Lys314Thr
CA126994
NM_001888.5:c.941A>C