Canonical Allele Identifier: PA2825112738
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2671917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1437Pro
CA389040144
NM_000257.4:c.4309G>C