Canonical Allele Identifier: PA1139679813
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 882707
ClinVar RCV Id: RCV001112595 RCV001112594 RCV001112596 RCV001279390 RCV001568541 RCV002482207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Thr624Met
CA224836137
NM_001127180.2:c.1871C>T