Canonical Allele Identifier: PA1139676506
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 864200
ClinVar RCV Id: RCV001071331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Ser1584Cys
CA381950857
NM_000260.4:c.4751C>G