Canonical Allele Identifier: PA915980586
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43224
ClinVar RCV Id: RCV000036128 RCV000267119 RCV000371726 RCV000324036 RCV000665330 RCV001034155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ile127Thr
CA132306
NM_001127180.2:c.380T>C