Canonical Allele Identifier: PA658662826
Gene: FA2H HGNC NCBI

Linked Data

ClinVar Variation Id: 449574
ClinVar RCV Id: RCV000520744 RCV003155224
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077282.3:p.Pro44Ser
CA396768354
NM_024306.5:c.130C>T