Canonical Allele Identifier: PA2828648135
Gene: CRYM HGNC NCBI

Linked Data

ClinVar Variation Id: 16934
ClinVar RCV Id: RCV000018442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363185.1:p.Lys314_Ter315insTyrAsnLysGlyThr
CA126992
NM_001376256.1:c.945A>T
CA395060442
NM_001376256.1:c.945A>C