Canonical Allele Identifier: PA2828320037
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 226432

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Leu640Pro
CA10576350
NM_001369365.1:c.1919T>C