Canonical Allele Identifier: PA1139673770
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 859133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser1037Tyr
CA389045508
NM_000257.4:c.3110C>A