Canonical Allele Identifier: PA1139679720
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 865814
ClinVar RCV Id: RCV001073328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ser508Pro
CA381935735
NM_001127180.2:c.1522T>C