Canonical Allele Identifier: PA915981201
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 196099
ClinVar RCV Id: RCV000665185 RCV000724054 RCV000988610 RCV001073919 RCV001171544 RCV002500491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ser1176Asn
CA242907
NM_001127180.2:c.3527G>A