Canonical Allele Identifier: PA915980629
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306161
ClinVar RCV Id: RCV000312582 RCV000352175 RCV000406232 RCV000606419 RCV001245525 RCV001833446
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Gln188Glu
CA6197170
NM_001127180.2:c.562C>G