Canonical Allele Identifier: PA2825115508
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1463810
ClinVar RCV Id: RCV001997799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Ser611Asn
CA6197625
NM_000260.4:c.1832G>A