Canonical Allele Identifier: PA915981109
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 178483
ClinVar RCV Id: RCV000155231 RCV000288323 RCV000345669 RCV000388720 RCV000974265 RCV004534989
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.His1029Arg
CA182416
NM_001127180.2:c.3086A>G