Canonical Allele Identifier: PA915980808
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 504950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Asn458Lys
CA6197486
NM_001127180.2:c.1374T>A
CA381935258
NM_001127180.2:c.1374T>G