Canonical Allele Identifier: PA2825113031
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072165
ClinVar RCV Id: RCV004012195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile1572Val
CA389037796
NM_000257.4:c.4714A>G