Canonical Allele Identifier: PA1139673753
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 919434

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1030His
CA257818692
NM_000257.4:c.3090A>C
CA389045650
NM_000257.4:c.3090A>T