Canonical Allele Identifier: PA2828320073
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2849875
ClinVar RCV Id: RCV003688039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Phe667Leu
CA381939379
NM_001369365.1:c.1999T>C
CA381939386
NM_001369365.1:c.2001C>A
CA381939387
NM_001369365.1:c.2001C>G