Canonical Allele Identifier: PA2825113146
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1743888
ClinVar RCV Id: RCV002340573

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn1633Lys
CA389037394
NM_000257.4:c.4899C>G
CA389037395
NM_000257.4:c.4899C>A