Canonical Allele Identifier: PA2828319431
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2741463
ClinVar RCV Id: RCV003555673

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Pro120Ser
CA6197119
NM_001369365.1:c.358C>T