Canonical Allele Identifier: PA915981248
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43215
ClinVar RCV Id: RCV000036119 RCV000665509 RCV000937221 RCV001111010 RCV001111011 RCV001002751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Cys1201Ser
CA132299
NM_001127180.2:c.3602G>C
CA381947024
NM_001127180.2:c.3601T>A