Canonical Allele Identifier: PA915980652
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 11851
ClinVar RCV Id: RCV000012625 RCV001047241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg212Cys
CA277962
NM_001127180.2:c.634C>T