Canonical Allele Identifier: PA2825627372
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43271
ClinVar RCV Id: RCV000036176 RCV000306975 RCV000366371 RCV000404997 RCV000724217 RCV001272803 RCV004534757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ala1665Val
CA132369
NM_001127180.2:c.4994C>T