Canonical Allele Identifier: PA099363
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 11851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg212Cys
CA277962
NM_000260.4:c.634C>T