Canonical Allele Identifier: PA137039
Gene: MYOZ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 45779
ClinVar RCV Id: RCV000039003 RCV001070182 RCV001170131 RCV002408523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057683.1:p.Thr6Ser
CA137037
NM_016599.5:c.17C>G
CA358203213
NM_016599.5:c.16A>T