Allele Registry

Canonical Allele Identifier: PA2499234434

Gene: P4HB HGNC NCBI

ClinVar Allele:

1158199

ClinVar RCV:

RCV001512301

RCV002495787

ClinVar Variation:

1165301

HGVS (amino-acid)	Matching Registered Transcripts
NP_000909.2:p.Ala144Thr	CA8842976 NM_000918.4:c.430G>A