Canonical Allele Identifier: PA915981354
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 235215
ClinVar RCV Id: RCV000224963 RCV001271756 RCV004020716
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ser1356Cys
CA6198306
NM_001127180.2:c.4066A>T