Canonical Allele Identifier: PA2828319519
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 11850
ClinVar RCV Id: RCV000665766 RCV001073914 RCV001221383 RCV003389443 RCV000012624 RCV000036232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Arg201His
CA277961
NM_001369365.1:c.602G>A