Canonical Allele Identifier: PA915980895
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 226432

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Leu651Pro
CA10576350
NM_001127180.2:c.1952T>C