Canonical Allele Identifier: PA237393
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 191731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr1019Ala
CA013327
NM_000257.4:c.3055A>G