Canonical Allele Identifier: PA915980682
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 11853
ClinVar RCV Id: RCV000012627 RCV003492291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg244Pro
CA121720
NM_001127180.2:c.731G>C