Canonical Allele Identifier: PA2499230254
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1060056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn238Lys
CA389052204
NM_000257.4:c.714C>G
CA389052205
NM_000257.4:c.714C>A